ClearanceBrief
510(k) K952038 ยท KCY Tourniquet, Pneumatic

CLEAN-CUFF

ApplicantInstrumed, Inc., Bothell WA, US
DecisionSubstantially Equivalent, Jul 11, 1995
ReceivedMay 1, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952038

DateFirm and productCodeLinked 510(k)
Sep 21, 2011Stryker Instruments Div. of Stryker Corporation
Stryker SmartPump Extension Tubing (Pneumatic tourniquet). Sterile tubing extension 40" and 60", set, luer lock. Rx only. Stryker Instruments Div. of Stryker Corporation. Optional accessories used wi
Terminated
KCYNone listed

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