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FDA 510(k) Application Details - K970534
Device Classification Name
System, Image Processing, Radiological
More FDA Info for this Device
510(K) Number
K970534
Device Name
System, Image Processing, Radiological
Applicant
MULTIMEDIA SOLUTIONS
1005 BEAU TERRE DRIVE,
SUITE 309
BENTONVILLE, AR 72712 US
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Contact
LAURENCE TRICE
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Regulation Number
892.2050
More FDA Info for this Regulation Number
Classification Product Code
LLZ
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More FDA Info for this Product Code
Date Received
02/12/1997
Decision Date
04/04/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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