ClearanceBrief
510(k) K960883 ยท GCJ Laparoscope, General & Plastic Surgery

INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8

ApplicantTaut, Inc., Geneva IL, US
DecisionSubstantially Equivalent, Mar 20, 1996
ReceivedMar 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960883

DateFirm and productCodeLinked 510(k)
Feb 15, 2007Taut, Inc.
Taut Intraducer Peritoneal Catheter, 12 Fr x 10 Fr x 20.3 cm; a sterile, Rx peritoneal catheter for single use, individually packaged in a Tyvek/clear pouch; Taut Inc., 2561 Kaneville Ct., Geneva, IL
Terminated
GBWNone listed

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