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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Columns, Glc
510(k) Number K791893
Device Name 19091-XXXXX SER. OF GLASS CAPILLARY COL.
Applicant
Hewlett-Packard Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Hewlett-Packard Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number862.2250
Classification Product Code
DII  
Date Received09/25/1979
Decision Date 10/30/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Toxicology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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