510(k) K993118 ยท FIE Needle, Fistula
BIOTEQUE A.V. FISTULA NEEDLE SET
| Applicant | Bioteque Corp., Flaggstaff AZ, US |
| Decision | Substantially Equivalent, Dec 17, 1999 |
| Received | Sep 20, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993118
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.