ClearanceBrief
510(k) K033584 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ARTHROCARE ARTHROWANDS

ApplicantArthrocare Corp., Sunnyvale CA, US
DecisionSubstantially Equivalent, Nov 28, 2003
ReceivedNov 13, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K033584

DateFirm and productCodeLinked 510(k)
Sep 19, 2008ArthroCare Corporation
ArthroCare ArthroWand Covator with Integrated Cable Wand, Catalog number AC4340-01. The product is a medical device for human use in electrosurgical cutting and coagulation accessories. Product is i
Terminated
GEINone listed

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