510(k) K834548 ยท FMF Syringe, Piston
HYPODERMIC SYRINGES & NEEDLES
| Applicant | Cordis Corp., Walker MI, US |
| Decision | Substantially Equivalent, Mar 6, 1984 |
| Received | Dec 27, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834548
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.