ClearanceBrief
510(k) K012640 ยท HRX Arthroscope

ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORIES, ELECTROSURGICAL WANDS

ApplicantMedical Instruments Technology, Inc., St. George UT, US
DecisionSubstantially Equivalent, Feb 28, 2002
ReceivedAug 13, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012640

DateFirm and productCodeLinked 510(k)
Sep 19, 2008Ascent Healthcare Solutions, Inc.
Turbovac Suction Wand - Reprocessed Sterile device -- Orthopedic Arthroscope.
Terminated
HRXNone listed

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