510(k) K161812 ยท FMF Syringe, Piston
Freedom Syringe
| Applicant | Procedure Products, Inc., Vancouver WA, US |
| Decision | Substantially Equivalent, Mar 27, 2017 |
| Received | Jul 1, 2016 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K161812
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.