# Advance Medical Device, Inc.

- Location (FDA's records): Camden, NJ
- FDA decisions: 5 (1990–1997): 5 510(k) clearances
- Product codes: JAF (1), JOP (1), HIB (1), DXN (1), DPT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K964697: Amd Home Health Monitor System and Amd Monitoring Station (Feb 11, 1997)
- K943200: Floscope Super Vascular Lab (Nov 21, 1995)
- K910441: Floscope Microdop (Mar 21, 1991)
- K905157: Floscope Vascular Lab. (Mar 15, 1991)
- K903744: Physician's Choice (Sep 12, 1990)

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