ClearanceBrief
510(k) K993411 ยท HIR Perineometer

FEMISCAN CLINIC SYSTEM, MODEL FS-ICTRA AND FEMISCAN PERSONAL SYSTEM, MODEL FS-HMTR

ApplicantMega Electronics , Ltd., East Longmeadow MA, US
DecisionSubstantially Equivalent, Jan 10, 2000
ReceivedOct 12, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993411

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.