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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original PMA or panel track supplement and may not represent the most recent labeling.
 
DeviceCOBE CENTRY(R) TPE SYSTEM
Generic NameSeparator, automated, blood cell and plasma, therapeutic
ApplicantGAMBRO BCT, INC.
10811 West Collins Ave.
Lakewood, CO 80215
PMA NumberP810023
Date Received05/18/1981
Decision Date03/16/1982
Withdrawal Date 10/09/2007
Product Code LKN 
Notice Date 04/09/1982
Advisory Committee Gastroenterology/Urology
Expedited Review Granted? No
Combination ProductNo
Supplements:  S002 
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