510(k) K062365 ยท FMF Syringe, Piston
ARTHREX ASPIRATE KIT
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Sep 29, 2006 |
| Received | Aug 14, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062365
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.