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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K844092
Device Name DIAGNOSTIC MICROSOPCE SLIDES
Applicant
Sybron Corp.
Portsmouth,  NH  03801
Applicant Contact HENRY N WILLIAMS
Correspondent
Sybron Corp.
Portsmouth,  NH  03801
Correspondent Contact HENRY N WILLIAMS
Date Received10/19/1984
Decision Date 10/25/1984
Decision Substantially Equivalent (SESE)
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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