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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Measuring, Lens Radius, Ophthalmic
510(k) Number K862517
Device Name BAUSCH & LOMB CONTACT LENS VIEWER
Applicant
Bausch & Lomb, Inc.
1400 N. Goodman St.
P.O.Box 450
Rochester,  NY  14692
Applicant Contact NICHOLAS A WALP
Correspondent
Bausch & Lomb, Inc.
1400 N. Goodman St.
P.O.Box 450
Rochester,  NY  14692
Correspondent Contact NICHOLAS A WALP
Regulation Number886.1430
Classification Product Code
HLF  
Date Received07/01/1986
Decision Date 08/11/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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