ClearanceBrief
510(k) K972894 ยท CAC Apparatus, Autotransfusion

AUTOTRANSFUSION APPARTUS (AUTOLOG)

ApplicantMedtronic Blood Management, Parker CO, US
DecisionSubstantially Equivalent, Apr 27, 1998
ReceivedAug 5, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972894

DateFirm and productCodeLinked 510(k)
Jun 30, 2010Medtronic Cardiovascular Revascularization & Surgical Therap
Hospital Grade Power Cord, UL, Part # 66319, 055476, manufactured by Electri-Cord Manufacturing Co. beginning in February 2003. The cords are a detachable unit, supplied with the instruments listed
Terminated
DWANone listed

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