510(k) K800462 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
PERCUTANEOUS INTRODUCER SET
| Applicant | Medical Components, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 19, 1980 |
| Received | Feb 29, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800462
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.