510(k) K894177 ยท FMF Syringe, Piston
NEEDLE*LESS DRUG VIAL ADAPTER
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Sep 12, 1989 |
| Received | Jun 15, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894177
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.