510(k) K100520 ยท FIE Needle, Fistula
NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER
| Applicant | Nipro Medical Corporation, Miami FL, US |
| Decision | Substantially Equivalent, Mar 17, 2010 |
| Received | Feb 23, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100520
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.