510(k) K821671 ยท FMF Syringe, Piston
DISPO. AES.
| Applicant | Hiraoka New York, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 28, 1982 |
| Received | Jun 7, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821671
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.