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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Chamber, Slide Culture
510(k) Number K781516
Device Name TEST SYSTEM TISSUE CELL CULTURE SLIDE
Applicant
Zeus Scientific, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Zeus Scientific, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number864.2240
Classification Product Code
KIY  
Date Received08/31/1978
Decision Date 09/27/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Pathology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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