Cardiac Ablation Percutaneous Catheter
Device class 3 · Review panel CV
FDA PMA supplement record
P930029/S072
RF Catheter Cables
Supplement S072 to premarket approval P930029. Product code LPB. Decision 1 July 2024.
Approval
Each row is one field of the openFDA record. The grey name is the field’s name in openFDA’s documentation.
| Field | Value | Field name |
|---|---|---|
| PMA number | P930029 | pma_number |
| Supplement number | S072 | supplement_number |
| Applicant | Medtronic, Inc. | applicant |
| Trade name | RF Catheter Cables | trade_name |
| Generic name | Cardiac ablation percutaneous catheter | generic_name |
| Product code | LPB | product_code |
| Advisory committee | Cardiovascular | advisory_committee_description |
| Date received | 2024-04-02 | date_received |
| Decision date | 2024-07-01 | decision_date |
| Decision code | APPR | decision_code |
| Supplement type | Real-Time Process | supplement_type |
| Supplement reason | Labeling Change - Indications/instructions/shelf life/tradename | supplement_reason |
Source: FDA openFDA, device/pma, P930029/S072, retrieved 2026-10-16 02:28 Eastern. Public domain (CC0).
Product code
The FDA classification record for the code on this record.
ArrHub vocabulary
Electrophysiology
LPB is one of the 61 product codes in ArrHub’s electrophysiology vocabulary, each held with its FDA classification record as its citation. Vocabulary entry verified 20 September 2026.
Supplement history
Every record of this PMA number in ArrHub’s verified view, newest first. Routine notices are listed, never summarised away.
| Record | Type | Reason | Decision |
|---|---|---|---|
| P930029/S072 FDA | Real-Time Process | Labeling Change - Indications/instructions/shelf life/tradename | 2024-07-01 |
| P930029/S071 FDA | 30-Day Notice | Process Change - Manufacturer/Sterilizer/Packager/Supplier | 2022-06-01 |
| P930029/S070 FDA | 30-Day Notice | Process Change - Manufacturer/Sterilizer/Packager/Supplier | 2021-12-07 |
| P930029/S069 FDA | 30-Day Notice | Process Change - Manufacturer/Sterilizer/Packager/Supplier | 2020-12-23 |
| P930029/S068 FDA | 30-Day Notice | Process Change - Manufacturer/Sterilizer/Packager/Supplier | 2020-12-15 |
| P930029/S067 FDA | 30-Day Notice | Process Change - Manufacturer/Sterilizer/Packager/Supplier | 2020-09-25 |
| P930029/S066 FDA | 30-Day Notice | Process Change - Manufacturer/Sterilizer/Packager/Supplier | 2020-07-23 |
| P930029/S065 FDA | Normal 180 Day Track | Labeling Change - Indications/instructions/shelf life/tradename | 2019-07-29 |
Source: FDA openFDA, device/pma, records of P930029, retrieved 2026-10-16 02:28 Eastern. 8 records in the verified view. Each identifier links to the FDA’s page.
ArrHub
What ArrHub adds to the record. Everything above this line is the agency’s; everything here is ArrHub’s, dated and attributed.
Record pair
No confirmed pair across the two registers for this record.
Resolved to
Medtronic
The register name above is resolved to its organisation under ArrHub’s alias table. Method: rule:normalize. Source: fda_applicant. Verified 20 September 2026.
Not yet in ArrHub’s weekly snapshot.
Raw record
The stored record exactly as ArrHub holds it, for anyone who wants to check the page against it.
Show the raw record (JSON)device/pma.json?search=pma_number:P930029+AND+supplement_number:S072&limit=1
{
"id": "b8b42e64-1c7d-4852-8886-371c6e3eac27",
"pma_key": "P930029/S072",
"pma_number": "P930029",
"supplement_number": "S072",
"applicant": "Medtronic, Inc.",
"trade_name": "RF Catheter Cables",
"generic_name": "Cardiac ablation percutaneous catheter",
"product_code": "LPB",
"advisory_committee_description": "Cardiovascular",
"decision_date": "2024-07-01",
"decision_code": "APPR",
"supplement_type": "Real-Time Process",
"supplement_reason": "Labeling Change - Indications/instructions/shelf life/tradename",
"date_received": "2024-04-02",
"source_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P930029&s=S072",
"verified_at": "2026-10-16T06:53:50.427+00:00",
"created_at": "2026-10-16T06:28:37.103881+00:00",
"collected_at": "2026-10-16T06:28:22.358+00:00",
"last_checked_at": "2026-10-16T06:53:50.427+00:00"
}The readable page is rendered from the record held in ArrHub’s verified view; the agency record at api.fda.gov governs where they differ.
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