# Novoste Corp.

- Location (FDA's records): Aguadilla, PR
- FDA decisions: 5 (1988–1995): 5 510(k) clearances
- Product codes: DQO (3), DYB (1), DQY (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
- K942977: Novoste Pulse Plus Blood Containment Device (Dec 28, 1995)
- K911527: Novoste Guiding Catheter (Apr 24, 1991)
- K900460: Modified Novoste Angiographic Catheter (Jul 17, 1990)
- K896690: Modified Angiographic Catheter (Jan 24, 1990)
- K875127: Novoste 4, 4.2, 5 and 6 French Catheters (Aug 9, 1988)

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