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FDA 510(k) Application Details - K151883
Device Classification Name
More FDA Info for this Device
510(K) Number
K151883
Device Name
5MP Monochrome LCD Monitor, RadiForce GX540
Applicant
EIZO CORPORATION
153 SHIMOKASHIWANO
HAKUSAN 924-8566 JP
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Contact
HIROAKI HASHIMOTO
Other 510(k) Applications for this Contact
Regulation Number
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Classification Product Code
PGY
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Date Received
07/09/2015
Decision Date
07/30/2015
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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