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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Multi-Analyte Controls, All Kinds (Assayed)
510(k) Number K022867
Device Name LINICAL PROTEIN 3 CALIBRATION VERIFIERS LEVELS A - E FOR THE BECKMAN-COULTER IMMAGE
Applicant
Cliniqa Corporation
1432 S. Mission Rd.
Fallbrook,  CA  92028
Applicant Contact CAROL RUGGIERO
Correspondent
Cliniqa Corporation
1432 S. Mission Rd.
Fallbrook,  CA  92028
Correspondent Contact CAROL RUGGIERO
Regulation Number862.1660
Classification Product Code
JJY  
Date Received08/28/2002
Decision Date 10/02/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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