Permanent Defibrillator Electrodes

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	NVY	product_code
Device name	Permanent Defibrillator Electrodes	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 NVY, 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
2026-08-19	Medtronic, Inc.	MEDTRONIC(R) TRANSVENE LEAD SYSTEM	P920015/S307 FDA
2026-06-24	Medtronic, Inc.	Sprint Quattro Lead (6946M)	P920015/S306 FDA
2026-04-24	Medtronic, Inc.	OmniaSecure™ MRI SureScan™ Lead Model 3930M	P240036/S006 FDA
2026-04-24	Medtronic, Inc.	OmniaSecure™ MRI SureScan™ Lead Model 3930M	P240036/S005 FDA
2026-04-15	Medtronic, Inc.	ACCESS 6717 KIT PIN PLUG (6717), DF-1 Connector Port Pin Plug (6719), IS-1 Connector Port Pin Plug Kit (6725), Sprint Qu (truncated in the FDA record)	P920015/S305 FDA
2026-03-09	Medtronic, Inc.	OmniaSecure™ MRI SureScan™ Lead Model 3930M	P240036/S004 FDA
2026-03-06	Medtronic, Inc.	HV Splitter/ Adaptor kit	P920015/S304 FDA
2026-02-13	Medtronic, Inc.	Sprint Quattro Lead (6935M, 6947); Sprint Quattro Lead (6935, 6947M)	P920015/S303 FDA
2026-02-10	Medtronic, Inc.	HV Splitter/Adaptor kit 5019 IS-1 Connector Port Pin Plug Kit 6725 Sprint Quattro Lead 6935, 6947 Sprint Quattro Lead 69 (truncated in the FDA record)	P920015/S302 FDA
2025-04-22	Medtronic, Inc.	OmniaSecure™ MRI SureScan™ Lead Model 3930M	P240036 FDA
1993-12-09	Medtronic, Inc.	MEDTRONIC(R) TRANSVENE LEAD SYSTEM	P920015 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

NVY 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:NVY

{
  "id": "fda_product_code:NVY",
  "vocabulary": "fda_product_code",
  "term": "NVY",
  "definition": "Permanent Defibrillator Electrodes",
  "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:NVY",
  "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": "2026-09-20T01:19:26.508288+00:00",
  "updated_at": "2026-09-20T01:19:12.218+00:00"
}

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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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