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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name interferential current therapy
510(k) Number K121662
Device Name VECTTOR VT-200
Original Applicant
6001-b s. staples st
corpus christi,  TX  78413
Original Contact donald a rhodes
Classification Product Code
Date Received06/05/2012
Decision Date 11/21/2012
Decision substantially equivalent (SESE)
510k Review Panel Ophthalmic
summary summary
Type Abbreviated
Reviewed by Third Party No
Combination Product No