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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Digital Image Communications, Radiological
510(k) Number K926315
Device Name PRACTICE PARTNER
Applicant
Rs Imaging
711 W. Kimberly Ave.
Suite 200
Placentia,  CA  92670
Applicant Contact SNYDER
Correspondent
Rs Imaging
711 W. Kimberly Ave.
Suite 200
Placentia,  CA  92670
Correspondent Contact SNYDER
Regulation Number892.2020
Classification Product Code
LMD  
Date Received12/15/1992
Decision Date 12/13/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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