510(k) K813461 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
PERCUTANEOUS ENTRY NEEDLE, SELDINGER
| Applicant | Ocean Medical Products, Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 29, 1981 |
| Received | Dec 11, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813461
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.