ClearanceBrief
510(k) K172796 ยท HET Laparoscope, Gynecologic (And Accessories)

Flex Robotic System and Flex Transabdominal Drive

ApplicantMedrobotics Corporation, Raynham MA, US
DecisionSubstantially Equivalent, Jan 18, 2018
ReceivedSep 15, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172796

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.