ClearanceBrief
510(k) K920340 ยท KKX Drape, Surgical, Antimicrobial

SUTURE REMOVAL KIT

ApplicantMedikmark, Inc., Chicago IL, US
DecisionUnknown, Apr 23, 1992
ReceivedJan 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920340

DateFirm and productCodeLinked 510(k)
Jul 22, 2004Medikmark, Incorporated
Staple Removal Tray/Set/Kit; a sterile Rx convenience kit containing a staple remover instrument, an alcohol prep pad, a PVP prep pad and a gauze sponge. Theses kits were marketed under the following
Terminated
KKXNone listed
Jul 22, 2004Medikmark, Incorporated
MediChoice Skin Staple Remover, reorder no. SSR 1001; a sterile Rx convenience kit containing a skin staple remover, a PVP prep pad and a 3 x 3 gauze sponge; 50 kits per case; Made for Owens & Minor
Terminated
KKXNone listed
Jul 22, 2004Medikmark, Incorporated
Staple Removal Set/Kit; a sterile Rx convenience kit containing a staple remover and a gauze sponge. Theses kits were marketed under the following labels, 50 kits per case: a) Medikmark inc. Staple R
Terminated
KKXNone listed

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