510(k) K913114 ยท FMF Syringe, Piston
TRIM-PORT(TM) IMPLANT ACCESS SYST DUAL TITAN PORT
| Applicant | Gerard Medical Enterprises, Inc., Charlton MA, US |
| Decision | Unknown, Jan 2, 1992 |
| Received | Jul 8, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913114
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.