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FDA 510(k) Application Details - K060349
Device Classification Name
System, Applicator, Radionuclide, Remote-Controlled
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510(K) Number
K060349
Device Name
System, Applicator, Radionuclide, Remote-Controlled
Applicant
NUCLETRON CORPORATION
8671 ROBERT FULTON DR.
COLUMBIA, MD 21046-2133 US
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Contact
LISA DIMMICK
Other 510(k) Applications for this Contact
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
02/10/2006
Decision Date
03/10/2006
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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