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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Manipulator, Plunger-Like Joint
510(k) Number K003185
Device Name FS ACTIVATOR III
Applicant
Activator Methods International, Ltd.
3714 E. Indian School Rd.
Phoenix,  AZ  85018
Applicant Contact ARLAN W FUHR
Correspondent
Activator Methods International, Ltd.
3714 E. Indian School Rd.
Phoenix,  AZ  85018
Correspondent Contact ARLAN W FUHR
Classification Product Code
LXM  
Date Received10/11/2000
Decision Date 03/20/2001
Decision Substantially Equivalent (SESE)
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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