ClearanceBrief
510(k) K171523 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Monopolar Single Use Laparoscopic Instrument

ApplicantGetsch+Hiller Medizintechnik GmbH, Tuttlingen, DE
DecisionSubstantially Equivalent, Aug 22, 2017
ReceivedMay 25, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171523

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.