# Rocap Div. of Sabratek Corp.

- Location (FDA's records): Orlando, FL
- FDA decisions: 3 (1999–1999): 3 510(k) clearances
- Product codes: FOZ (3)
- 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
- K990390: Heparin IV Flush Syringe, 10 U/ML  \ (Dec 10, 1999)
- K990308: Rocap Heparin IV Flush Syringe, 100U/ML (Dec 10, 1999)
- K984614: Normal Saline Flush Syringe (May 27, 1999)

Source page: https://510kreport.com/company/rocap-div-of-sabratek