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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Muscle, Powered
510(k) Number K912342
Device Name DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM
Applicant
Amer Inst of Electrodiagnosis/Electrotherapy, Inc.
435 W. 57th St.Enue
Apt. 3l
New York,  NY  10019
Applicant Contact W. T LIBERSON
Correspondent
Amer Inst of Electrodiagnosis/Electrotherapy, Inc.
435 W. 57th St.Enue
Apt. 3l
New York,  NY  10019
Correspondent Contact W. T LIBERSON
Regulation Number890.5850
Classification Product Code
IPF  
Date Received05/24/1991
Decision Date 12/09/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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