ClearanceBrief
510(k) K984240 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ENDOPATH ENDOSCOPIC INSTRUMENTS

ApplicantEthicon Endo-Surgery, Inc., Cincinnati OH, US
DecisionSubstantially Equivalent, Jun 22, 1999
ReceivedNov 27, 1998
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K984240

DateFirm and productCodeLinked 510(k)
Jan 29, 2008Ethicon Endo-Surgery Inc
Ethicon Endopath 5 mm Curved Dissector with Monopolar Cautery, Product Code: 5DCD, Ethicon Endo-Surgery, Inc, Cincinatti, OH 45242
Terminated
GDINone listed

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