# Bt Medical Co., Inc.

- Location (FDA's records): Bridgeport, PA
- FDA decisions: 6 (1992–2003): 6 510(k) clearances
- Names in FDA's records: Bt Medical Co., Inc. (5); Bt Medical (1)
- Product codes: IPF (2), JAA (2), NBW (1), EAJ (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Bayer Corp.: 1 (https://510kreport.com/company/bayer)

## Recent decisions
- K032029: BTG Smartest Glucose Test System (Dec 18, 2003)
- K931268: Ureteral Compression Device (Jul 19, 1993)
- K930885: Pneumatic Compression Device (Jul 13, 1993)
- K931269: Lead Apron (Jun 2, 1993)
- K915321: BTM-200 (Proposed) Powered Muscle Stimulator (Jul 17, 1992)
- K914999: BTM-100 Powered Muscle Stimulator (Proposed) (Apr 23, 1992)

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