510(k) K063368 ยท FIE Needle, Fistula
NIPRO BIOHOLE NEEDLE
| Applicant | Nipro Medical Corp., Miami FL, US |
| Decision | Substantially Equivalent, Feb 5, 2007 |
| Received | Nov 7, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063368
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.