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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name projector, ophthalmic
510(k) Number K781658
Device Name PROJECTOR, ACCU-CHART ACUITY
Applicant
BAUSCH & LOMB, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
BAUSCH & LOMB, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number886.1680
Classification Product Code
HOS  
Date Received09/28/1978
Decision Date 10/17/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
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