ClearanceBrief
510(k) K945633 ยท GWG Endoscope, Neurological

NEURO CHANNEL ENDOSCOPE MODEL 2232

ApplicantClarus Medical Systems, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Sep 19, 1995
ReceivedNov 16, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945633

DateFirm and productCodeLinked 510(k)
Jul 20, 2004Medtronic Neurosurgery
Channel Neuroendoscope, Standard Resolution, 21.6 cm. Catalog No. 2232-001
Terminated
GWGNone listed

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