510(k) K003193 ยท FMF Syringe, Piston
DUPLOGRIP
| Applicant | Baxter Healthcare Corp, Glendale CA, US |
| Decision | Substantially Equivalent, Nov 7, 2000 |
| Received | Oct 12, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003193
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.