FDA 510(k) Application Details - K192065

Device Classification Name System,Planning,Radiation Therapy Treatment

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510(K) Number K192065
Device Name System,Planning,Radiation Therapy Treatment
Applicant Siemens Medical Solutions USA, Inc.
2501 N Barrington Rd.
Hoffman Estates, IL 60192 US
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Contact Veronica Padharia
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Regulation Number 892.5050

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Classification Product Code MUJ
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Date Received 08/01/2019
Decision Date 09/18/2019
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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