510(k) K882238 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
VESSEL DILATOR AND INTRODUCER SHEATH
| Applicant | Ideal Medical, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Aug 25, 1988 |
| Received | May 27, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882238
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.