510(k) K881073 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
SHILEY FEMORAL CANNULAE INTRODUCER KIT
| Applicant | Shiley, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jun 9, 1988 |
| Received | Mar 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881073
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.