510(k) K963171 ยท DQX Wire, Guide, Catheter
CINCH QR SGW EXTENSION
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Nov 7, 1996 |
| Received | Aug 14, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963171
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.