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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name set, lens, trial, ophthalmic
510(k) Number K873907
Device Name CONFIRMATION TESTS
Applicant
RICHMOND PRODUCTS, INC.
1021 SO ROGERS CIRCLE
BOCA RATON,  FL  33487 -2894
Applicant Contact LLOYD POWELL
Correspondent
RICHMOND PRODUCTS, INC.
1021 SO ROGERS CIRCLE
BOCA RATON,  FL  33487 -2894
Correspondent Contact LLOYD POWELL
Regulation Number886.1405
Classification Product Code
HPC  
Date Received09/25/1987
Decision Date 12/29/1987
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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