ClearanceBrief
510(k) K990766 ยท IKN Electromyograph, Diagnostic

CERSR ELECTROMYOGRAPHY SYSTEM

ApplicantParaspinal Diagnostic Corp., Rockville MD, US
DecisionSubstantially Equivalent, Aug 27, 1999
ReceivedMar 8, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990766

DateFirm and productCodeLinked 510(k)
Jun 30, 2010SpineMatrix Inc
Lumbar Matrix Scan, Diagnostic Electromyography System consisting of the CERSR Electromyography System and Electrode Array; the system consists of two devices. The first is a system of capital equipm
Terminated
IKNNone listed

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