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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Lipase-Esterase, Enzymatic, Photometric, Lipase
510(k) Number K874640
Device Name WAKO(TM) AUTOKIT LIPASE
Applicant
WAKO CHEMICALS, USA, INC.
12300 FORD RD.
SUITE 130
DALLAS,  TX  75234
Applicant Contact TOSHIHIKO ODA
Correspondent
WAKO CHEMICALS, USA, INC.
12300 FORD RD.
SUITE 130
DALLAS,  TX  75234
Correspondent Contact TOSHIHIKO ODA
Regulation Number862.1465
Classification Product Code
CHI  
Date Received11/12/1987
Decision Date 12/22/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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