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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K852603
Device Name MCCOY'S 5A MEDIUM - POWDERED FORM
Applicant
Mediatech, Inc.
13884 Park Center Rd.
Herndon,  VA  20171
Applicant Contact ROBERT R TASCHNER
Correspondent
Mediatech, Inc.
13884 Park Center Rd.
Herndon,  VA  20171
Correspondent Contact ROBERT R TASCHNER
Date Received06/19/1985
Decision Date 07/12/1985
Decision Substantially Equivalent (SESE)
510k Review Panel Pathology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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