510(k) K895203 ยท FMF Syringe, Piston
EN-TRAP SYRINGE
| Applicant | The Medtech Group, Inc., South Planifield NJ, US |
| Decision | Substantially Equivalent, Oct 18, 1989 |
| Received | Aug 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895203
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.