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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 K930670
Device Name PHYACTION 787
Applicant
Verimed Holdings, Inc.
1401 E. Broward Blvd.
Suite 200
Fort Lauderdale,  FL  33301
Applicant Contact CHRISTOPHER CHASE
Correspondent
Verimed Holdings, Inc.
1401 E. Broward Blvd.
Suite 200
Fort Lauderdale,  FL  33301
Correspondent Contact CHRISTOPHER CHASE
Regulation Number890.5850
Classification Product Code
IPF  
Date Received02/09/1993
Decision Date 07/02/1993
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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