# Medtronic Andover Medical, Inc.

- Location (FDA's records): Haverhill, MA
- FDA decisions: 6 (1985–1991): 6 510(k) clearances
- Product codes: DRX (3), DSA (1), LDD (1), GXY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Vanguard Medical Concepts, Inc.: 1 (https://510kreport.com/company/vanguard-medical-concepts)

## Its most-cited devices
- K882174: Modified Model 5455 Disposable Surgical Cable (1988), cited by 1

## Recent decisions
- K910494: Resting Ekg Electrode Series (Apr 22, 1991)
- K905446: Meditronic Andover Medical Model 1690 Electrode (Feb 5, 1991)
- K903018: Medtronic Andover Medical Saf-D-Fib Model 1220-002 (Dec 3, 1990)
- K903554: Nortech Model 87202204 Electrode (Aug 30, 1990)
- K882174: Modified Model 5455 Disposable Surgical Cable (Jul 22, 1988)
- K852469: Saf-D-Fib (Sep 16, 1985)

Source page: https://510kreport.com/company/medtronic-andover-medical