510(k) K083454 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
NUOVOCATH
| Applicant | U.S. Safety Syringes Co., Inc., Crofton MD, US |
| Decision | Substantially Equivalent, Dec 4, 2008 |
| Received | Nov 21, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083454
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.