FDA 510(k) Applications Submitted by AMERICAN RADIOSURGERY, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K101220 05/03/2010 EXPLORER 4D TREATMENT PLANNING SYSTEM AMERICAN RADIOSURGERY, INC.
K060314 02/08/2006 ROTATING GAMMA SYSTEM. GAMMA ART-6000 AMERICAN RADIOSURGERY, INC.
K093588 11/19/2009 EXPLORER 4D TREATMENT PLANNING SYSTEM AMERICAN RADIOSURGERY, INC.


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