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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 K874591
Device Name ILLUMINATING INFUSION CONTACT LENS FOR EYE SURGERY
Applicant
Vitreo Dynamics, Co.
684 Capewood Pl.
Southaven,  MS  38671
Applicant Contact JEFF FREEMAN
Correspondent
Vitreo Dynamics, Co.
684 Capewood Pl.
Southaven,  MS  38671
Correspondent Contact JEFF FREEMAN
Classification Product Code
HPX  
Date Received11/09/1987
Decision Date 05/03/1988
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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