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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cyanomethemoglobin
510(k) Number K821202
Device Name HEMOGLOBIN REAGENT SET
Applicant
OMEGA MEDICAL ELECTRONICS
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
OMEGA MEDICAL ELECTRONICS
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number864.7500
Classification Product Code
GKK  
Date Received04/27/1982
Decision Date 05/24/1982
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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