510(k) K052267 ยท FIE Needle, Fistula
SUPERCATH V
| Applicant | Togo Medikit Co., Ltd., Tokyo, JP |
| Decision | Substantially Equivalent, Oct 27, 2006 |
| Received | Aug 19, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052267
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.