ClearanceBrief
510(k) K090309 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

LAGIS ENDOSCOPIC INSTRUMENTS

ApplicantLagis Enterprises Co, Ltd., Houston TX, US
DecisionSubstantially Equivalent, Aug 28, 2009
ReceivedFeb 6, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090309

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.