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FDA 510(k) Application Details - K022389
Device Classification Name
Source, Brachytherapy, Radionuclide
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510(K) Number
K022389
Device Name
Source, Brachytherapy, Radionuclide
Applicant
WORLDWIDE MEDICAL TECHNOLOGIES, LLC
426 MAIN ST. NORTH
WOODBURY, CT 06798-0505 US
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Contact
RICK TERWILLIGER
Other 510(k) Applications for this Contact
Regulation Number
892.5730
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Classification Product Code
KXK
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More FDA Info for this Product Code
Date Received
07/23/2002
Decision Date
05/06/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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