510(k) K063613 ยท FMF Syringe, Piston
MODIFICATION TO TERUMO SYRINGE WITH/WITHOUT NEEDLE
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Dec 26, 2006 |
| Received | Dec 5, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K063613
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.