510(k) K963388 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
VESSEL DILATOR
| Applicant | Maxxim Medical, Fort Worth TX, US |
| Decision | Substantially Equivalent, Mar 11, 1997 |
| Received | Aug 28, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963388
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.