510(k) K871148 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
URESIL CAROTID ARTERY SIZERS
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Apr 22, 1987 |
| Received | Mar 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871148
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.