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FDA 510(k) Application Details - K953911
Device Classification Name
System, Image Processing, Radiological
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510(K) Number
K953911
Device Name
System, Image Processing, Radiological
Applicant
PHILIPS MEDICAL SYSTEMS, INC.
710 BRIDGEPORT AVE.
P.O. BOX 860
SHELTON, CT 06484 US
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Contact
PETER ALTMAN
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Regulation Number
892.2050
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Classification Product Code
LLZ
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More FDA Info for this Product Code
Date Received
08/21/1995
Decision Date
06/27/1996
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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