# Qmed, Inc.

- Location (FDA's records): Louisville, KY
- FDA decisions: 11 (1984–1998): 11 510(k) clearances
- Product codes: DPS (2), GXY (1), DXG (1), DSI (1), GEI (1), DXN (1), LOS (1), DRX (1), HAM (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (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 whose devices it cites most
- Spacelabs, Inc.: 1 (https://510kreport.com/company/spacelabs)

## Firms that cite its devices most
- Dyansys, Inc.: 1 (https://510kreport.com/company/dyansys)
- Medtechs, LLC: 1 (https://510kreport.com/company/medtechs)
- Boston Medical Technologies, Inc.: 1 (https://510kreport.com/company/boston-medical-technologies)
- Atcor Medical: 1 (https://510kreport.com/company/atcor-medical)

## Its most-cited devices
- K972991: Monitor One NDX (1998), cited by 4

## Recent decisions
- K972991: Monitor One NDX (Dec 3, 1998)
- K932109: Profilomat (Dec 3, 1993)
- K921476: Interp-1000 (Oct 21, 1992)
- K897121: Qekg Electrocardiograph (Apr 30, 1990)
- K873591: A.R.M. (Aspen Return Monitor) (Sep 30, 1987)
- K862377: Qmed Self Adhering Electrode (Sep 26, 1986)
- K863091: Bicord by Qmed (Aug 29, 1986)
- K861437: Qmed System 2150 (May 20, 1986)

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