FDA 510(k) Applications for Medical Device Product Code "KRI"
(Accessory Equipment, Cardiopulmonary Bypass)

FDA 510(k) Number Applicant Device Name Decision Date
K020365 3T MEDICAL SYSTEMS, LLC. 3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE 05/03/2002
K992635 STOECKERT INSTRUMENTE INTERFACE MODULE IDDD 12/20/1999
K990512 STOECKERT INSTRUMENTE STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS 11/23/1999


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