510(k) K904476 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
VESSEL DILATOR
| Applicant | Datascope Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Dec 10, 1990 |
| Received | Oct 1, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904476
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.