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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Antigens, Cf (Including Cf Control), Influenza Virus A, B, C
510(k) Number K884191
Device Name INFLUENZA A IFA TEST FOR DIRECT ANTIGEN DETECTION
Applicant
Baxter Diagnostics, Inc.
P.O. Box 520672
Miami,  FL  33152
Applicant Contact HOWARD TAYLOR
Correspondent
Baxter Diagnostics, Inc.
P.O. Box 520672
Miami,  FL  33152
Correspondent Contact HOWARD TAYLOR
Regulation Number866.3330
Classification Product Code
GNX  
Date Received10/06/1988
Decision Date 11/22/1988
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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