510(k) K030571 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
ACUVANCE PLUS SAFETY IV CATHETER, PROTECTIV PLUS SAFETY IV CATHETER, OPTIVA IV CATHETER
| Applicant | Ethicon Endo-Surgery, Inc., Cincinnati OH, US |
| Decision | Substantially Equivalent, Mar 28, 2003 |
| Received | Feb 24, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030571
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.