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FDA 510(k) Application Details - K092439
Device Classification Name
More FDA Info for this Device
510(K) Number
K092439
Device Name
CANON DIGITAL FLUOROSCOPY AND RADIOGRAPHY, MODEL CXDI-50RF
Applicant
VIRTUAL IMAGING, INC.
333 MILFORD RD.
DEERFIELD, IL 60015 US
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Contact
DANIEL KAMM
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
OWB
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/10/2009
Decision Date
11/30/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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