FDA 510(k) Application Details - K193562

Device Classification Name

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510(K) Number K193562
Device Name AI-Rad Companion Organs RT
Applicant Siemens Medical Solutions USA, Inc.
40 Liberty Blvd. Mail Code 65-3
Malvern, PA 19355 US
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Contact Lauren Bentley
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Regulation Number

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Classification Product Code QKB
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Date Received 12/23/2019
Decision Date 11/06/2020
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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