510(k) K922101 ยท DQO Catheter, Intravascular, Diagnostic
ANGIOGRAPHIC CATHETER -- MODIFICATION
| Applicant | Interventional Therapeutics Corp., South San Francisco CA, US |
| Decision | Substantially Equivalent, Feb 12, 1993 |
| Received | May 6, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922101
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.