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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Source, Carrier, Fiberoptic Light
510(k) Number K841731
Device Name BRIMFIELD FIBEROPTIC LIGHT SCOURCE
Applicant
BRIMFIELD SCIENTIFIC INSTRUMENTS
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
BRIMFIELD SCIENTIFIC INSTRUMENTS
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number874.4350
Classification Product Code
EQH  
Date Received04/26/1984
Decision Date 07/16/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
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