# K990308: Rocap Heparin IV Flush Syringe, 100U/ML

- Pathway: 510(k) (Traditional)
- Applicant: Rocap Div. of Sabratek Corp.
- Decided: Dec 10, 1999 after 312 days
- Product code: FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The ROCAP Heparin Flush Syringe 100 U/mL is indicated for use to maintain patency of indwelling venous access devices.

Source page: https://510kreport.com/device/K990308
Methodology: https://510kreport.com/methodology