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FDA 510(k) Application Details - K072171
Device Classification Name
Accelerator, Linear, Medical
More FDA Info for this Device
510(K) Number
K072171
Device Name
Accelerator, Linear, Medical
Applicant
VISION RT LIMITED
1244 FAIRWAY VALLEY COURT
LINCOLN, CA 95648 US
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Contact
ROBERT J MORTON, M.S.
Other 510(k) Applications for this Contact
Regulation Number
892.5050
More FDA Info for this Regulation Number
Classification Product Code
IYE
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/06/2007
Decision Date
10/01/2007
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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