510(k) K883073 ยท FMF Syringe, Piston
N.M.D.C. USER PROTECTIVE HYPODERMIC SYRINGE SYSTEM
| Applicant | National Medical Device Corp., Valley Stream NY, US |
| Decision | Substantially Equivalent, Feb 28, 1989 |
| Received | Jul 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883073
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.