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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)
510(k) Number K897021
Device Name MARTIN-HENSLEY SEGMENT LENS
Applicant
Bruce W. Martin O.D. and Edward Hensley
P.O. Box 386
Gladwin,  MI  48624
Applicant Contact MARTIN, OD
Correspondent
Bruce W. Martin O.D. and Edward Hensley
P.O. Box 386
Gladwin,  MI  48624
Correspondent Contact MARTIN, OD
Classification Product Code
HPX  
Date Received12/19/1989
Decision Date 06/22/1990
Decision Substantially Equivalent (SESE)
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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