meddevicedb.com FDA Device Reference

trophon Wireless Ultrasound Probe Holder

K241536 Class II Traditional
Decision Date
2024-09-27
Sponsor / Applicant
Nanosonics Limited

Technical Specification

510(k) Submission ID K241536
Product Code OUJ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2024-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

trophon Wireless Ultrasound Probe Holder received FDA 510(k) clearance under submission number K241536, sponsored by Nanosonics Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code OUJ and 21 CFR 892.1570, within the Radiology review panel as a Class II device.