ClearanceBrief
510(k) K232270 ยท JOW Sleeve, Limb, Compressible

DVT Motion Pneumatic Compression Device

ApplicantKoge Micro Tech Co., Ltd., New Taipei, TW
DecisionSubstantially Equivalent, Mar 6, 2024
ReceivedJul 31, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232270

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.