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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 K950402
Device Name CORSINI 9090
Applicant
C.A.T. DI Corsini G. & C. Spa
Via Pila 3/3
40044 - Pontecchio Marconi(Bo),  IT 40044
Applicant Contact FRANCESCO BIANCO
Correspondent
C.A.T. DI Corsini G. & C. Spa
Via Pila 3/3
40044 - Pontecchio Marconi(Bo),  IT 40044
Correspondent Contact FRANCESCO BIANCO
Regulation Number892.1980
Classification Product Code
IXR  
Date Received02/01/1995
Decision Date 03/31/1995
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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