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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Microtiter Diluting/Dispensing
510(k) Number K810022
Device Name SRD III
Applicant
Dynatech Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Dynatech Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.2500
Classification Product Code
JTC  
Date Received01/05/1981
Decision Date 01/26/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
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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