510(k) K032292 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
BIOTEQUE A.V. FISTULA NEEDLE SET WITH SAFETY FLEX
| Applicant | Bioteque Corp., Flagstaff AZ, US |
| Decision | Substantially Equivalent, Mar 22, 2004 |
| Received | Jul 24, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032292
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.