FDA 510(k) Application Details - K910710

Device Classification Name Source, Brachytherapy, Radionuclide

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510(K) Number K910710
Device Name Source, Brachytherapy, Radionuclide
Applicant BEST ASSOC. CORP.
7643 FULLERTON RD.
SPRINGFIELD, VA US
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Contact SANKARA I RAMASWAMY
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Regulation Number 892.5730

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Classification Product Code KXK
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Date Received 02/20/1991
Decision Date 06/10/1991
Decision SE - Substantially Equivalent
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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