510(k) K001616 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
MODIFICATION TO SYRINGE PREFILLED WITH 0.9% SODIUM CHLORIDE
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Jul 27, 2000 |
| Received | May 25, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001616
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.