ClearanceBrief
510(k) K982984 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ACCUSHEAR LAPAROSCOPIC SURGICAL INSTRUMENTS

ApplicantMicroline Pentax, Inc., Wellesley MA, US
DecisionSubstantially Equivalent, Oct 21, 1998
ReceivedAug 26, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982984

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.