ClearanceBrief
510(k) K123553 ยท KCY Tourniquet, Pneumatic

ZIMMER A.T.S. 4000TS AUTOMATIC TOURNIQUET SYSTEM

ApplicantZimmer, Inc., Indianpolis IN, US
DecisionSubstantially Equivalent, Aug 9, 2013
ReceivedNov 19, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123553

DateFirm and productCodeLinked 510(k)
Jul 27, 2017Zimmer Surgical Inc
A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on tho
Terminated
KCYNone listed

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