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Dolphin Medical Imaging USB Ultrasound System

K192573 Class II Traditional
Decision Date
2019-11-19
Sponsor / Applicant
Dolphin Medical Imaging, LLC

Technical Specification

510(k) Submission ID K192573
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 2019-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dolphin Medical Imaging USB Ultrasound System received FDA 510(k) clearance under submission number K192573, sponsored by Dolphin Medical Imaging, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2019-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.