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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 K893803
Device Name FEVER LINE AND FEVER LINE PLUS
Applicant
Liquid Crystal Sciences, Inc.
105/120 Interstate N.
Pkwy. E.
Atlanta,  GA  30339
Applicant Contact L BRETT
Correspondent
Liquid Crystal Sciences, Inc.
105/120 Interstate N.
Pkwy. E.
Atlanta,  GA  30339
Correspondent Contact L BRETT
Regulation Number880.2200
Classification Product Code
KPD  
Date Received05/22/1989
Decision Date 08/21/1989
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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