ClearanceBrief
510(k) K052067 ยท JAF Monitor, Ultrasonic, Nonfetal

DOPPLER GUIDED PROCTOSCOPE, MODEL 500H

ApplicantMultigon Industries, Inc., Yonkers NY, US
DecisionSubstantially Equivalent, Aug 29, 2005
ReceivedAug 1, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K052067

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.