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Clarius Ultrasound Scanner

K213436 Class II Special
Decision Date
2021-11-15
Sponsor / Applicant
Clarius Mobile Health Corp.

Technical Specification

510(k) Submission ID K213436
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2021-11-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Clarius Ultrasound Scanner received FDA 510(k) clearance under submission number K213436, sponsored by Clarius Mobile Health Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2021-11-15.

Classification & Regulation

This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.