510(k) K060095 ยท FMF Syringe, Piston
MODIFICATION TO: VACLOK SYRINGE
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Feb 10, 2006 |
| Received | Jan 13, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060095
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.