FDA 510(k) Application Details - K181279

Device Classification Name System, X-Ray, Stationary

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510(K) Number K181279
Device Name System, X-Ray, Stationary
Applicant Siemens Medical Solutions, Inc.
40 Liberty Boulevard 65-1A
Malvern, PA 19355 US
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Contact Denise Adams
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Regulation Number 892.1680

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Classification Product Code KPR
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Date Received 05/15/2018
Decision Date 06/13/2018
Decision SESE - SUBST EQUIV
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review



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