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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 K892960
Device Name LINDQUIST MODEL SS POWERED MUSCLE STIMULATOR
Applicant
R.J. Lindquist Co.
2419 W. 9th St.
Los Angeles,  CA  90006
Applicant Contact ROBIN K BISARYA
Correspondent
R.J. Lindquist Co.
2419 W. 9th St.
Los Angeles,  CA  90006
Correspondent Contact ROBIN K BISARYA
Regulation Number890.5850
Classification Product Code
IPF  
Date Received04/25/1989
Decision Date 08/02/1990
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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