# Cape Tech Medical Products

- Location (FDA's records): Falmouth, MA
- FDA decisions: 3 (1992–1993): 3 510(k) clearances
- Product codes: KNQ (1), LQR (1), KNY (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
- K926038: Flex-Tech Balloon Dilator (Oct 25, 1993)
- K926039: Guide-Tech Encapsulated Guidewire (Aug 5, 1993)
- K926040: Heli-Tech Retrieval Basket (Dec 23, 1992)

Source page: https://510kreport.com/company/cape-tech-medical-products