meddevicedb.com FDA Device Reference

RS85 Diagnostic Ultrasound System

K240516 Class II Traditional
Decision Date
2024-06-12
Sponsor / Applicant
Samsung Medison Co., Ltd.

Technical Specification

510(k) Submission ID K240516
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2024-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RS85 Diagnostic Ultrasound System received FDA 510(k) clearance under submission number K240516, sponsored by Samsung Medison Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-06-12.

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.