# Adam Spencer Corp.

- Location (FDA's records): Miami, FL
- FDA decisions: 2 (1997–1997): 2 510(k) clearances
- Product codes: DQO (2)
- 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
- K963092: Maxi-Torque Plus Softip Angiographic Catheter (Jan 13, 1997)
- K964331: Asc High Pressure Braided Tubes (Jan 13, 1997)

Source page: https://510kreport.com/company/adam-spencer