ClearanceBrief
510(k) K081102 ยท GWG Endoscope, Neurological

VSU - VISIONSENSE STEREOSCOPIC VISION SYSTEM

ApplicantVisionsense, Ltd., Washington DC, US
DecisionSubstantially Equivalent, May 29, 2008
ReceivedApr 17, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081102

DateFirm and productCodeLinked 510(k)
Mar 8, 2012Visionsense, Ltd.
Visionsense Stereoscopic Vision System, Brand name VSII, Model/Part Numbers 172-0030 and 172-0040 --- Classification Name: Neurological Endoscope --- NOTE: Model Numbers 172-0032, 172-0044, 172-0070,
Terminated
GWGNone listed

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