510(k) K925632 ยท DQO Catheter, Intravascular, Diagnostic
BALT GUIDING CATHETER
| Applicant | Target Therapeutics, Freemont CA, US |
| Decision | Substantially Equivalent, Jun 29, 1993 |
| Received | Nov 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925632
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.