Cardiac Ablation Percutaneous Catheter

FDA product classification. Device class 3. Review panel CV.

Classification

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
Product code	LPB	product_code
Device name	Cardiac Ablation Percutaneous Catheter	device_name
Device class	3	device_class
Review panel	CV	review_panel
Regulation number	empty	regulation_number
Medical specialty	Unknown	medical_specialty

Source: FDA openFDA, device/classification, product code LPB, as held in ArrHub’s controlled vocabulary with its citation. Public domain (CC0).

PMA records with this code

Every verified record ArrHub holds under the code, newest first.

Decision	Applicant	Device	Record
2026-09-03	Irvine Biomedical, Inc.	Therapy™ (including Bi-Directional and 4mm Thermistor) Ablation Catheter	P040014/S052 FDA
2026-08-07	St Jude Medical	Ampere Generator	P960016/S094 FDA
2026-08-07	Irvine Biomedical, Inc.	Ampere Generator	P040014/S051 FDA
2026-07-31	Stereotaxis, Inc.	MAGiC Ablation Catheter	P240014/S001 FDA
2026-04-23	Medtronic Cryocath, LP	Freezor 207Fl,207F3,207F5, Freezor Xtra 217Fl,217F3,217F5	P020045/S113 FDA
2026-01-15	St Jude Medical	Livewire™ TC XLS™	P960016/S093 FDA
2026-01-05	Stereotaxis, Inc.	MAGiC Ablation Catheter	P240014 FDA
2005-01-14	Irvine Biomedical, Inc.	IBI THERAPY CARDIAC ABLATION SYSTEM ERS/ 1500T RF GENERATOR	P040014 FDA
2003-04-17	Medtronic Cryocath, LP	7F FREEZOR CARDIAC CRYOABLATION CATHETER AND CCT.2 CRYOCONSOLE SYSTEM	P020045 FDA
1999-05-04	St Jude Medical	LIVEWIRE(R) CARDIAC ABLATION SYSTEM	P960016 FDA

510(k) clearances with this code

Every verified record ArrHub holds under the code, newest first.

None in the verified view.

ArrHub

What ArrHub adds to the record. Everything above this line is the agency’s; everything here is ArrHub’s, dated and attributed.

ArrHub vocabulary

Electrophysiology

LPB is one of the 56 product codes in ArrHub’s electrophysiology vocabulary, each held with its FDA classification record as its citation. Vocabulary entry verified 20 September 2026.

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/classification.json?search=product_code:LPB

{
  "id": "fda_product_code:LPB",
  "vocabulary": "fda_product_code",
  "term": "LPB",
  "definition": "Cardiac Ablation Percutaneous Catheter",
  "attrs": {
    "device_class": "3",
    "review_panel": "CV",
    "medical_specialty": "Unknown",
    "regulation_number": ""
  },
  "jurisdiction": "US",
  "authority": "FDA",
  "ep_relevant": true,
  "source_url": "https://api.fda.gov/device/classification.json?search=product_code:LPB",
  "verified_by": "Bruno Deslauriers",
  "verified_at": "2026-09-20T01:22:27.524165+00:00",
  "notes": "Fetched from https://open.fda.gov/apis/device/classification/",
  "created_at": "2026-09-20T01:19:10.339347+00:00",
  "updated_at": "2026-09-20T01:18:56.037+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.

Links open the agency’s own records. Unlabelled links open web pages. Links marked (JSON) open an agency’s data record, which a browser shows as plain text.

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