# Vascucare, Inc.

- Location (FDA's records): Orangeburg, NY
- FDA decisions: 3 (1988–1989): 3 510(k) clearances
- Product codes: DWB (1), BZQ (1), LYK (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
- K890047: Vascucare Percutaneous Angioscopy Delivery System (Jun 20, 1989)
- K883158: Respiratory Airway Tube Monitor (Ratm) (Mar 6, 1989)
- K881780: Vascucare Angiopump (Sep 28, 1988)

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