510(k) K920177 ยท DQF Actuator, Syringe, Injector Type
VERSA-VIAL
| Applicant | Bioteque America, Inc., Levittown PA, US |
| Decision | Substantially Equivalent, Jul 13, 1992 |
| Received | Jan 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920177
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.