ClearanceBrief
510(k) K960004 ยท FDX Endoscopic Cytology Brush

CELL RECOVERY SYSTEM

ApplicantMedical Device Technologies, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Mar 20, 1996
ReceivedJan 2, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960004

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.