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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name unit, phacofragmentation
510(k) Number K830474
Device Name IV STAND
Applicant
TEKNAR, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
TEKNAR, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number886.4670
Classification Product Code
HQC  
Date Received02/15/1983
Decision Date 04/05/1983
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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