FDA 510(k) Application Details - K192496

Device Classification Name System, Nuclear Magnetic Resonance Imaging

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510(K) Number K192496
Device Name System, Nuclear Magnetic Resonance Imaging
Applicant Siemens Medical Solutions USA Inc.
40 Liberty Boulevard, Mail Code 65-IA
Malvern, PA 19355 US
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Contact Cordell L Fields
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Regulation Number 892.1000

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Classification Product Code LNH
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Date Received 09/11/2019
Decision Date 02/28/2020
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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