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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Formalin, Neutral Buffered
510(k) Number K872663
Device Name DRY-FORM
Applicant
Anatech, Ltd.
1020 Harts Lake Rd.
Battle Creek,  MI  49015
Applicant Contact FELDMAN, M.S.
Correspondent
Anatech, Ltd.
1020 Harts Lake Rd.
Battle Creek,  MI  49015
Correspondent Contact FELDMAN, M.S.
Regulation Number864.4010
Classification Product Code
IFP  
Date Received07/08/1987
Decision Date 08/06/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Pathology
510k Review Panel Pathology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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