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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Ring, Ophthalmic (Flieringa)
510(k) Number K832912
Device Name GELENDER VACUUM FIXATION RING SYS
Applicant
MIAMI EYE TECHNOLOGY, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
MIAMI EYE TECHNOLOGY, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number886.4350
Classification Product Code
HNH  
Date Received08/29/1983
Decision Date 01/10/1984
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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