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Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro)

K241979 Class II Special
Decision Date
2024-08-22
Sponsor / Applicant
Beijing Konted Medical Technology Co.,Ltd

Technical Specification

510(k) Submission ID K241979
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2024-08-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro) received FDA 510(k) clearance under submission number K241979, sponsored by Beijing Konted Medical Technology Co.,Ltd. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-08-22.

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.