# American Medical Technology, Inc.

- Location (FDA's records): Brooklyn, CT
- FDA decisions: 6 (1987–1997): 6 510(k) clearances
- Product codes: FMI (1), ITI (1), KKX (1), LYK (1), BTM (1), FPK (1)
- Predicates its devices cite: 2 (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 whose devices it cites most
- Quickie Designs, Inc.: 1 (https://510kreport.com/company/quickie-designs)
- Invacare Corp.: 1 (https://510kreport.com/company/invacare)

## Firms that cite its devices most
- American Bantex Corp.: 1 (https://510kreport.com/company/american-bantex)

## Its most-cited devices
- K963808: Choice Powered Wheelchair (1997), cited by 1

## Recent decisions
- K963808: Choice Powered Wheelchair (Feb 12, 1997)
- K905745: Ametec Masy Modular Angioscope System (Apr 23, 1992)
- K874567: Resuscitator (Feb 29, 1988)
- K874430: Needle Container (Jan 4, 1988)
- K874360: Plastic Tubing Connector (Nov 17, 1987)
- K873313: Surgical Drape (Sep 4, 1987)

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