510(k) K893546 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
OPTICALLY CLEAR RADIOPAQUE CATHETER
| Applicant | Critikon Company, LLC, Tampa FL, US |
| Decision | Substantially Equivalent, Nov 1, 1989 |
| Received | May 11, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893546
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.