ClearanceBrief
510(k) K843247 ยท ITX Transducer, Ultrasonic, Diagnostic

KOI PACHYMETER

ApplicantKoi, Inc., Frazer PA, US
DecisionSubstantially Equivalent, Apr 30, 1986
ReceivedAug 20, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843247

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.