510(k) K955111 ยท DQO Catheter, Intravascular, Diagnostic
MAXI-TORQUE PLUS ANGIOGRAPHIC CATHETER
| Applicant | Adam Spence Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 31, 1996 |
| Received | Nov 8, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955111
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.