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FDA 510(k) Application Details - K022635
Device Classification Name
System, Applicator, Radionuclide, Remote-Controlled
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510(K) Number
K022635
Device Name
System, Applicator, Radionuclide, Remote-Controlled
Applicant
NUCLETRON CORPORATION
7080 COLUMBIA GATEWAY DR.
COLUMBIA, MD 21046-2133 US
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Contact
LISA DIMMICK
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Regulation Number
892.5700
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Classification Product Code
JAQ
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More FDA Info for this Product Code
Date Received
08/08/2002
Decision Date
09/06/2002
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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