ClearanceBrief
510(k) K030551 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ARTHROCARE CONTROLLER (SYSTEM 2000 AND 8000); ARTHROCARE PATIENT CABLE; FOOT CONTROL; POWER CORD; WANDS

ApplicantArthrocare Corp., Sunnyvale CA, US
DecisionSubstantially Equivalent, Mar 7, 2003
ReceivedFeb 21, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K030551

DateFirm and productCodeLinked 510(k)
Aug 30, 2009ArthroCare Corporation
ArthroWand Saber 30 with Integrated Cable wand, Catalog number AC4330-01, Manufactured by ArthroCare Corporation, Sunnyvale, CA
Terminated
GEINone listed

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