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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 K802775
Device Name FIBER OPTIC ADAPTER #60-0896
Applicant
ASPEN LABORATORIES, INC.
MD 
Correspondent
ASPEN LABORATORIES, INC.
MD 
Regulation Number874.4350
Classification Product Code
EQH  
Date Received11/03/1980
Decision Date 12/16/1980
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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