ClearanceBrief
510(k) K233500 ยท HIH Hysteroscope (And Accessories)

Benesta Tissue Removal Device

ApplicantCaldera Medical, Inc., Westlake Village CA, US
DecisionSubstantially Equivalent, Nov 30, 2023
ReceivedOct 31, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K233500

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.