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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name lens, contact, polymethylmethacrylate, diagnostic
510(k) Number K872855
Device Name 18MM PEYMAN WIDE FIELD YAG LASER LENS
Applicant
OCULAR INSTRUMENTS, INC.
12100 NORTHUP WAY
SUITE D
BELLEVUE,  WA  98005
Applicant Contact TAMSIN J ERICKSON
Correspondent
OCULAR INSTRUMENTS, INC.
12100 NORTHUP WAY
SUITE D
BELLEVUE,  WA  98005
Correspondent Contact TAMSIN J ERICKSON
Regulation Number886.1385
Classification Product Code
HJK  
Date Received07/17/1987
Decision Date 09/04/1987
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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