510(k) K932420 ยท DQO Catheter, Intravascular, Diagnostic
SCIMED 6 FR., 7 FR., AND 8 FR.,TRIGUIDE GUIDING
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Aug 17, 1993 |
| Received | May 19, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932420
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.