510(k) K833460 ยท FMF Syringe, Piston
SYRINGE,PISTON NEEDLE, HOLLOW LUMEN
| Applicant | Aldrich Chemical Co., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 28, 1983 |
| Received | Oct 5, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833460
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.