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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Light, Fiber Optic, Dental
510(k) Number K801592
Device Name FIBER OPTIC HOSE
Applicant
Lares Manufacturing Co., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Lares Manufacturing Co., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number872.4620
Classification Product Code
EAY  
Date Received07/11/1980
Decision Date 07/21/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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