ClearanceBrief
510(k) K031639 ยท HEX Colposcope (And Colpomicroscope)

INTERMED ZOOM COLPOSCOPE

ApplicantIntermed Group, Inc., Lake Worth FL, US
DecisionSubstantially Equivalent, Aug 22, 2003
ReceivedMay 27, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031639

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.