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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Biofeedback
510(k) Number K883597
Device Name MYODAC
Applicant
THOUGHT TECHNOLOGY LTD.
2180 BELGRAVE AVE.
MONTREAL, QUEBEC,  CA H4A 2L8
Applicant Contact HAL K MYERS
Correspondent
THOUGHT TECHNOLOGY LTD.
2180 BELGRAVE AVE.
MONTREAL, QUEBEC,  CA H4A 2L8
Correspondent Contact HAL K MYERS
Regulation Number882.5050
Classification Product Code
HCC  
Date Received08/22/1988
Decision Date 11/16/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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