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FDA 510(k) Application Details - K033093
Device Classification Name
System, Image Processing, Radiological
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510(K) Number
K033093
Device Name
System, Image Processing, Radiological
Applicant
CONNEXMD
8536 18TH AVENUE NW
SEATTLE, WA 98117 US
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Contact
CURTIS LEBLEU
Other 510(k) Applications for this Contact
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
09/29/2003
Decision Date
11/05/2003
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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