510(k) K820384 ยท FMF Syringe, Piston
GLASS SYRINGES, DRUG, LUER LOCK
| Applicant | Procedure Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 15, 1982 |
| Received | Feb 9, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820384
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.