510(k) K933183 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SCIMED VIPER
| Applicant | Scimed Life Systems, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 9, 1993 |
| Received | Jun 30, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933183
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.