FDA 510(k) Application Details - K870662

Device Classification Name Stimulator, Nerve, Ac-Powered

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510(K) Number K870662
Device Name Stimulator, Nerve, Ac-Powered
Applicant LIFE-TECH INTL., INC.
P.O. BOX 36221
HOUSTON, TX US
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Contact ANDREW C KYLE
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Regulation Number 868.2775

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Classification Product Code BXM
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Date Received 02/19/1987
Decision Date 10/28/1987
Decision SE - Substantially Equivalent
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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