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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Kit, Screening, Trichomonas
510(k) Number K852665
Device Name SYNCOR TRICH DIRECT IMMUNOFLUORESCENCE ASSAY
Applicant
Syncor Intl. Corp.
1440 Fourth St.
Berkeley,  CA  94710
Applicant Contact TERRY D SMITH
Correspondent
Syncor Intl. Corp.
1440 Fourth St.
Berkeley,  CA  94710
Correspondent Contact TERRY D SMITH
Regulation Number866.2660
Classification Product Code
JWZ  
Date Received06/24/1985
Decision Date 08/13/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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