510(k) K101708 ยท FMF Syringe, Piston
PATIENT SAFE LUER CAP
| Applicant | Retractable Technologies, Inc., Little Elm TX, US |
| Decision | Substantially Equivalent, Feb 24, 2011 |
| Received | Jun 17, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101708
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.