510(k) K062979 ยท FCG Biopsy Needle
THYROSAMPLER
| Applicant | Acd Medical Innovation Corp., Littleton CO, US |
| Decision | Substantially Equivalent, May 30, 2007 |
| Received | Sep 29, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062979
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.