510(k) K984614 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
NORMAL SALINE FLUSH SYRINGE
| Applicant | Rocap Div. of Sabratek Corp., Orlando FL, US |
| Decision | Substantially Equivalent, May 27, 1999 |
| Received | Dec 29, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984614
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.