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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, High Pressure Liquid Chromatography
510(k) Number K935666
Device Name PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP
Applicant
The Perkin-Elmer Corp.
761 Main Ave.
Norwalk,  CT  06859
Applicant Contact JOHN KENT
Correspondent
The Perkin-Elmer Corp.
761 Main Ave.
Norwalk,  CT  06859
Correspondent Contact JOHN KENT
Regulation Number862.2260
Classification Product Code
KIE  
Date Received11/26/1993
Decision Date 04/26/1994
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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