meddevicedb.com FDA Device Reference

THD REVOLUTION

K141657 Class II Traditional
Decision Date
2015-02-24
Sponsor / Applicant
Thd Spa

Technical Specification

510(k) Submission ID K141657
Product Code JAF
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1540
Decision Date 2015-02-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THD REVOLUTION received FDA 510(k) clearance under submission number K141657, sponsored by Thd Spa. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2015-02-24.

Classification & Regulation

This clearance is catalogued under FDA product code JAF and 21 CFR 892.1540, within the Radiology review panel as a Class II device.