meddevicedb.com FDA Device Reference

trophon2

K173865 Class II Traditional
Decision Date
2018-04-24
Sponsor / Applicant
Nanosonics Limited

Technical Specification

510(k) Submission ID K173865
Product Code OUJ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2018-04-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

trophon2 received FDA 510(k) clearance under submission number K173865, 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 2018-04-24.

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.