510(k) K964331 ยท DQO Catheter, Intravascular, Diagnostic
ASC HIGH PRESSURE BRAIDED TUBES
| Applicant | Adam Spencer Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 13, 1997 |
| Received | Oct 30, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964331
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.