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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 may have changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
DeviceCOBE CENTRY(R) TPE SYSTEM
Classification Nameseparator, automated, blood cell and plasma, therapeutic
Generic Nameseparator, automated, blood cell and plasma, therapeutic
Applicant
GAMBRO 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[ Registered Establishments with LKN ]
Notice Date 04/09/1982
Advisory Committee Gastroenterology/Urology
Expedited Review Granted? No
Combination Product No
Supplements: S002 
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