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FDA 510(k) Application Details - K102476
Device Classification Name
Digitizer, Image, Radiological
More FDA Info for this Device
510(K) Number
K102476
Device Name
Digitizer, Image, Radiological
Applicant
VIDAR SYSTEMS CORP.
365 HERNDON PARKWAY
HERNDON, VA 20170 US
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Contact
CARRIE L BRANCART
Other 510(k) Applications for this Contact
Regulation Number
892.2030
More FDA Info for this Regulation Number
Classification Product Code
LMA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/30/2010
Decision Date
10/07/2010
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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