# Andover Medical, Inc.

- Location (FDA's records): Lawrence, MA
- FDA decisions: 21 (1976–1991): 21 510(k) clearances
- Product codes: DRX (8), GXY (3), DRO (2), KRB (2), DYG (2), DPS (1), DSH (1), CAT (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Lorenz Biotech S.P.A.: 1 (https://510kreport.com/company/lorenz-biotech)

## Its most-cited devices
- K831785: Neuro Ease (1983), cited by 1

## Recent decisions
- K905729: Canmed 451 (Feb 7, 1991)
- K903427: Nortech Model 86901000 Electrode (Aug 17, 1990)
- K885171: Modified Label Change to Model 5455 Surgical Cable (Jan 12, 1989)
- K860636: Fastrace Iii, Ecg Electrode (May 9, 1986)
- K854433: Ecg Monitoring/Defibrillation Electrode (May 8, 1986)
- K860535: Unilateral Oxygen Delivery System (Ulods) (Apr 1, 1986)
- K860283: Ami Cardio-Pad (Mar 31, 1986)
- K843410: Flow-Directed Pediatric Thermodil- Cath (Nov 20, 1984)

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