510(k) K896096 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
SOLOSTICK (AMPLATZ DILATOR NEEDLE)
| Applicant | Microvena Corp., Findley MN, US |
| Decision | Substantially Equivalent, Apr 10, 1990 |
| Received | Oct 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896096
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.