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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 K093259
Device Name ARP RX100
Applicant
ARP MANUFACTURING, INC
4655 KIRKWOOD COURT
boulder,  CO  80301
Applicant Contact lewis ward
Correspondent
REGULATORY TECHNOLOGY SERVICES, LLC
1000 Westgate Drive,
Suite 510k
saint paul,  MN  55114
Correspondent Contact mark job
Regulation Number890.5850
Classification Product Code
IPF  
Date Received10/19/2009
Decision Date 12/17/2009
Decision substantially equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
summary summary
Type Traditional
Reviewed by Third Party Yes
Combination Product No
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