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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Accelerator, Linear, Medical
510(k) Number K894722
Device Name RENNER-PLAN
Applicant
W.D. Renner Consulting Co.
6771 E. Pleasant Run Pky., S.
Dr.
Indianapolis,  IN  46219
Applicant Contact DEAN RENNER
Correspondent
W.D. Renner Consulting Co.
6771 E. Pleasant Run Pky., S.
Dr.
Indianapolis,  IN  46219
Correspondent Contact DEAN RENNER
Regulation Number892.5050
Classification Product Code
IYE  
Date Received07/25/1989
Decision Date 01/03/1990
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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