ClearanceBrief
510(k) K013668 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

BERCHTOLD ELEKTROTOM 106 HITT

ApplicantBerchtold Corp., Altadena CA, US
DecisionSubstantially Equivalent, Feb 4, 2002
ReceivedNov 6, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013668

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.