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FDA 510(k) Application Details - K022354
Device Classification Name
System, X-Ray, Tomography, Computed
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510(K) Number
K022354
Device Name
System, X-Ray, Tomography, Computed
Applicant
ULTRAGUIDE LTD.
377 ROUTE 17 SOUTH
HASBROUCK HEIGHTS, NJ 07601 US
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Contact
GEORGE MYERS
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Regulation Number
892.1750
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Classification Product Code
JAK
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More FDA Info for this Product Code
Date Received
07/19/2002
Decision Date
08/13/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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