ClearanceBrief
510(k) K951072 ยท GKP Instrument, Coagulation, Automated

PROTIME MICROCOAGULATION SYSTEM

ApplicantInternational Technidyne Corp., Edison NJ, US
DecisionSubstantially Equivalent, Oct 27, 1995
ReceivedMar 8, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951072

DateFirm and productCodeLinked 510(k)
Jan 25, 2008International Technidyne Corporation
ProTime Microcoagulation System Instrument:Catalogue Number: PROTIMEINT, International Technidyne Corporation (ITC), Piscataway, NJ 08854
Terminated
GJSNone listed
Jan 13, 2007International Technidyne Corp.
International Technidyne Corporation (ITC) ProTime Microcoagulation System Instrument-Catalogue Number-Protimeint & Protimepro, Protimeintrf & Protimeprorf, Protimeintl & Protimeprol.
Terminated
GJSNone listed

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