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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Test, Time, Partial Thromboplastin
510(k) Number K801460
Device Name PACIFIC HEMOSTASIS THROMBO-SCREEN KAPTT
Applicant
PACIFIC HEMOSTASIS
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
PACIFIC HEMOSTASIS
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number864.7925
Classification Product Code
GGW  
Date Received06/24/1980
Decision Date 07/28/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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