ClearanceBrief
510(k) K944547 ยท GWF Stimulator, Electrical, Evoked Response

DANTEC KEYPOINT

ApplicantMckenna & Cuneo, Washington DC, US
DecisionSubstantially Equivalent, Sep 19, 1995
ReceivedSep 15, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K944547

DateFirm and productCodeLinked 510(k)
May 25, 2013Alpine Biomed Aps
Natus neurology Dantec KEYPOINT.NET 2.20. Catalog/Part Numbers: 9031A070103, 9031A006502, 9033A071103, 9033A072102, 9031A070102, 9033A007402, 9033A071102, 9033A072103, 9033A0701, 9033A0711HA, 9033A071
Terminated
GWFNone listed

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