# Bistech, Inc.

- Location (FDA's records): Ayer, MA
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: EOQ (1)
- Predicates its devices cite: 2 (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
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Plastimed Laboratoire Pharmaceutique: 1 (https://510kreport.com/company/plastimed-laboratoire-pharmaceutique)

## Recent decisions
- K024165: Dual-Lumen Catheter (Jan 10, 2003)

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