510(k) K926344 ยท KNY Accessories, Catheter, G-U
HYDROPHILIC COATED GUIDEWIRE
| Applicant | Surgitek, Racine WI, US |
| Decision | Substantially Equivalent, Mar 5, 1993 |
| Received | Dec 17, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926344
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.