ClearanceBrief
510(k) K932922 ยท MED Sterilant, Medical Devices

PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR

ApplicantCottrell, Ltd., Englewood CO, US
DecisionSubstantially Equivalent, Jul 3, 1995
ReceivedJun 15, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932922

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.