510(k) K863936 ยท IWR Holder, Syringe, Lead
DUFFY BOLUS INJECTOR
| Applicant | Viox Corp., Seattle WA, US |
| Decision | Substantially Equivalent, Jan 6, 1987 |
| Received | Oct 9, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863936
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.