FDA 510(k) Application Details - K161136

Device Classification Name System,Planning,Radiation Therapy Treatment

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510(K) Number K161136
Device Name System,Planning,Radiation Therapy Treatment
Applicant ACCURAY INCORPORATED
1310 CHESAPEAKE TERRACE
SUNNYVALE, CA 94089 US
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Contact Shweta Kaushik
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Regulation Number 892.5050

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Classification Product Code MUJ
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Date Received 04/22/2016
Decision Date 06/24/2016
Decision SESE - SUBST EQUIV
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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