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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K872737
Device Name PERKIN-ELMER LC235 DIODE ARRAY DETECTOR
Applicant
The Perkin-Elmer Corp.
CT  06856
Applicant Contact RAYMOND M TRENCK
Correspondent
The Perkin-Elmer Corp.
CT  06856
Correspondent Contact RAYMOND M TRENCK
Date Received07/09/1987
Decision Date 09/18/1987
Decision Substantially Equivalent (SESE)
510k Review Panel Toxicology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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