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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Radiographic, Tilting
510(k) Number K884531
Device Name BETA 90/50 MOBILE IMAGING TABLE
Applicant
Beta Medical Products Co.
100 Lincoln St.
Akron,  OH  44308
Applicant Contact KEVIN BENOIT
Correspondent
Beta Medical Products Co.
100 Lincoln St.
Akron,  OH  44308
Correspondent Contact KEVIN BENOIT
Regulation Number892.1980
Classification Product Code
IXR  
Date Received10/28/1988
Decision Date 01/11/1989
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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