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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K820125
Device Name COBE CENTRY 2000 RX
Applicant
Cobe Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Cobe Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Date Received01/18/1982
Decision Date 03/23/1982
Decision Substantially Equivalent (SESE)
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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