ClearanceBrief
510(k) K922881 ยท GEX Powered Laser Surgical Instrument

CLARUS MODELS 1100, 1101, 1102, 1103 LASER DISC

ApplicantClarus Medical Systems, Inc., Minneapolis MN, US
DecisionUnknown, Nov 16, 1992
ReceivedJun 16, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922881

DateFirm and productCodeLinked 510(k)
Jul 27, 2021Clarus Medical, Llc
Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
Terminated
GEXNone listed

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