510(k) K934988 ยท DQY Catheter, Percutaneous
9 FRENCH LARGE LUMEN TRIGUIDE PLUS GUIDING CATHETER
| Applicant | Scimed Life Systems, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jan 14, 1994 |
| Received | Oct 18, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934988
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.