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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Controller, Infusion, Intravascular, Electronic
510(k) Number K812233
Device Name RATEMINDER
Applicant
Anatros Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Anatros Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.5725
Classification Product Code
LDR  
Date Received08/11/1981
Decision Date 08/25/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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