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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Strip, Temperature, Forehead, Liquid Crystal
510(k) Number K770517
Device Name NF DEVICE
Applicant
Rpr, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Rpr, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.2200
Classification Product Code
KPD  
Date Received03/18/1977
Decision Date 07/15/1977
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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