510(k) K072345 ยท FMF Syringe, Piston
POWRSYRINGE MONITOR
| Applicant | Pinyons Medical Technology, Inc., Park City UT, US |
| Decision | Substantially Equivalent, Sep 21, 2007 |
| Received | Aug 21, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072345
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.