510(k) K014088 ยท FMF Syringe, Piston
DUPLOREACH
| Applicant | Baxter Healthcare Corp, Glendale CA, US |
| Decision | Substantially Equivalent, Jun 7, 2002 |
| Received | Dec 12, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014088
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.