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FDA 510(k) Application Details - K960911
Device Classification Name
System, Digital Image Communications, Radiological
More FDA Info for this Device
510(K) Number
K960911
Device Name
System, Digital Image Communications, Radiological
Applicant
SCIMAGE, INC.
25500 CRESCENT LN.
LOS ALTOS, CA 94022-4521 US
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Contact
SAI P RAYA
Other 510(k) Applications for this Contact
Regulation Number
892.2020
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Classification Product Code
LMD
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More FDA Info for this Product Code
Date Received
03/06/1996
Decision Date
05/29/1996
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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