510(k) K063721 ยท FIE Needle, Fistula
NIPRO SAFETOUCH II GAMMA
| Applicant | Nipro Medical Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 12, 2007 |
| Received | Dec 15, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K063721
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.