# Vasocor, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 3 (1997–2002): 3 510(k) clearances
- Product codes: JOM (2), DXN (1)
- Predicates its devices cite: 3 (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
- Life Sciences Manufacturing, Inc.: 1 (https://510kreport.com/company/life-sciences-manufacturing)
- Touritu Engineering Co., Inc.: 1 (https://510kreport.com/company/touritu-engineering)
- Hypertension Diagnostics, Inc.: 1 (https://510kreport.com/company/hypertension-diagnostics)

## Recent decisions
- K011625: Vasocor Vascular Diagnostic Center (Model 300) (Jan 23, 2002)
- K990123: PVR-100/Vasogram (Apr 12, 1999)
- K973659: Vasocor PVR 100 (Dec 17, 1997)

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