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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K852423
Device Name TIMENTIN 85MCG SENSITIVITY DISC
Applicant
Difco Laboratories, Inc.
P. O. Box 331058
Detroit,  MI  48232 -7058
Applicant Contact ROBERT
Correspondent
Difco Laboratories, Inc.
P. O. Box 331058
Detroit,  MI  48232 -7058
Correspondent Contact ROBERT
Date Received06/07/1985
Decision Date 07/16/1985
Decision Substantially Equivalent (SESE)
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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