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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Enzymatic Radiochemical Assay, Amikacin
510(k) Number K833546
Device Name MODIFICATION OF EMIT AND AMIKACIN ASSAY
Applicant
Syva Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Syva Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number862.3035
Classification Product Code
LDN  
Date Received10/14/1983
Decision Date 12/08/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Toxicology
510k Review Panel Toxicology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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