ClearanceBrief
510(k) K922391 ยท HRX Arthroscope

ENDOSCOPIC CARPAL TUNNEL INSTRUMENTS

ApplicantInstratek, Inc., Houston TX, US
DecisionSubstantially Equivalent, Aug 18, 1992
ReceivedMay 20, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922391

DateFirm and productCodeLinked 510(k)
Apr 30, 2019Stryker GmbH
Endotrac ECTR Hook/Triangle Blade Kit, Catalogue Number 2056-1
Terminated
HRXNone listed
Apr 30, 2019Stryker GmbH
Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1
Terminated
HRXNone listed

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