510(k) K953805 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
0.9% SODIUM CHLORIDE DILUENT IN PLASTIC SYRINGE
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Jun 28, 1996 |
| Received | Aug 8, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953805
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.