ClearanceBrief
510(k) K896134 ยท GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

ACUFLO, VACUUM-POWERED BODY FLUID SUCTION APPARA.

ApplicantGoosen Enterprises, Inc., Goldenrod FL, US
DecisionSubstantially Equivalent, Aug 30, 1990
ReceivedOct 24, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896134

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.