# Andromed, Inc.

- Location (FDA's records): Saint Laurent, Quebec, CA
- FDA decisions: 5 (2000–2005): 5 510(k) clearances
- Product codes: DQD (4), BZQ (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
- Masimo Corporation: 1 (https://510kreport.com/company/masimo)

## Its most-cited devices
- K021389: Biological Sound Monitor (BSM) Sensor (2002), cited by 1

## Recent decisions
- K051779: Androflow - Respiratory Rate Monitor (Sep 30, 2005)
- K021389: Biological Sound Monitor (BSM) Sensor (Oct 1, 2002)
- K022298: I-Stethos Link (Oct 1, 2002)
- K010729: Agilent Electronic Stethoscope, Models M4532A and M4533A (Oct 26, 2001)
- K001306: Stethos, Model Stxxyyzz or 001 XXX, Stethos Link, Model Slxxyyzz or 002 XXX (Jul 20, 2000)

Source page: https://510kreport.com/company/andromed