510(k) K963092 ยท DQO Catheter, Intravascular, Diagnostic
MAXI-TORQUE PLUS SOFTIP ANGIOGRAPHIC CATHETER
| Applicant | Adam Spencer Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 13, 1997 |
| Received | Aug 8, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963092
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.