Permanent Pacemaker Electrode

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	DTB	product_code
Device name	Permanent Pacemaker Electrode	device_name
Device class	3	device_class
Review panel	CV	review_panel
Regulation number	870.3680	regulation_number
Medical specialty	Cardiovascular	medical_specialty

Source: FDA openFDA, device/classification, product code DTB, 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
2026-04-15	Medtronic, Inc.	Myocardial Pacing Lead	P120017/S040 FDA
2026-02-20	Medtronic, Inc.	Myocardial Pacing Lead	P120017/S039 FDA
2015-04-27	Medtronic, Inc.	MODEL 5071 LEAD	P120017 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

DTB 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:DTB

{
  "id": "fda_product_code:DTB",
  "vocabulary": "fda_product_code",
  "term": "DTB",
  "definition": "Permanent Pacemaker Electrode",
  "attrs": {
    "device_class": "3",
    "review_panel": "CV",
    "medical_specialty": "Cardiovascular",
    "regulation_number": "870.3680"
  },
  "jurisdiction": "US",
  "authority": "FDA",
  "ep_relevant": true,
  "source_url": "https://api.fda.gov/device/classification.json?search=product_code:DTB",
  "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": "2026-09-20T01:09:14.770762+00:00",
  "updated_at": "2026-09-20T01:19:02.36+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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