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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name aid, vision image intensification
510(k) Number K863994
Device Name VIEWSCAN
Applicant
SENSORY AIDS CORP.
205 WEST GRAND AVENUE,
SUITE 122
BENSENVILLE,  IL  60106
Applicant Contact RON B MERRICK
Correspondent
SENSORY AIDS CORP.
205 WEST GRAND AVENUE,
SUITE 122
BENSENVILLE,  IL  60106
Correspondent Contact RON B MERRICK
Regulation Number886.5910
Classification Product Code
HOT  
Date Received10/14/1986
Decision Date 10/31/1986
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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