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FDA 510(k) Application Details - K040995
Device Classification Name
System, X-Ray, Stationary
More FDA Info for this Device
510(K) Number
K040995
Device Name
System, X-Ray, Stationary
Applicant
ANALOGIC CORP.
8 CENTENNIAL DR.
PEABODY, MA 01960 US
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Contact
DONALD J SHERRATT
Other 510(k) Applications for this Contact
Regulation Number
892.1680
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Classification Product Code
KPR
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More FDA Info for this Product Code
Date Received
04/16/2004
Decision Date
05/25/2004
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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