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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K781097
Device Name INOCULUM STDIZING SYS., INOCUPAC
Applicant
3M Company
8124 Pacific Ave.
White City,  OR  97503
Correspondent
3M Company
8124 Pacific Ave.
White City,  OR  97503
Date Received07/03/1978
Decision Date 08/14/1978
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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