510(k) K945850 ยท FIE Needle, Fistula
BRAUN DIACAN(R) FISTULA NEEDLES
| Applicant | B. Braun of America, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Oct 6, 1995 |
| Received | Nov 30, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945850
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.