FDA 510(k) Application Details - K190314

Device Classification Name System, Imaging, Pulsed Echo, Ultrasonic

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510(K) Number K190314
Device Name System, Imaging, Pulsed Echo, Ultrasonic
Applicant MedNovel Technology Ltd
1154 Cadillac Court
Milpitas, CA 95035 US
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Contact Jia Yu
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Regulation Number 892.1560

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Classification Product Code IYO
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Date Received 02/13/2019
Decision Date 10/09/2019
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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