ClearanceBrief
510(k) K926140 ยท KDP Regulator, Vacuum

VACUUM POWER BODY FLUID SUCTION APPARATUS

ApplicantHill-Rom, Inc., Batesville TN, US
DecisionSubstantially Equivalent, Jul 27, 1993
ReceivedDec 7, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926140

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.