ClearanceBrief
510(k) K000480 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ACTIVE ELECTRODE MONITORING SYSTEM

ApplicantElectroscope, Inc., Indian Hills CO, US
DecisionSubstantially Equivalent, May 2, 2000
ReceivedFeb 14, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000480

DateFirm and productCodeLinked 510(k)
Jul 24, 2003Encision, Inc.
EM2 NC AEM Monitor (NON-COM)
Terminated
GEINone listed
Jul 24, 2003Encision, Inc.
EM2+A NC AEM Monotor (NON-COM)
Terminated
GEINone listed
Jul 24, 2003Encision, Inc.
EM2M NC AEM Monitor, (NON-COM)
Terminated
GEINone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.