510(k) K911656 ยท CAC Apparatus, Autotransfusion
PLEUR-EVAC PLUS CONTIN. REINFUS. & AUTOINFUS. SYST
| Applicant | Pfizer Hospital Products Group, Inc., Fall River MA, US |
| Decision | Substantially Equivalent, Aug 13, 1991 |
| Received | Apr 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911656
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.