meddevicedb.com FDA Device Reference

INNOCURE IMRT FILTER (COMPENSATORS)

K052383 Class II Traditional
Decision Date
2006-03-29
Sponsor / Applicant
Innocure, LLC

Technical Specification

510(k) Submission ID K052383
Product Code IXI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5710
Decision Date 2006-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INNOCURE IMRT FILTER (COMPENSATORS) received FDA 510(k) clearance under submission number K052383, sponsored by Innocure, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-03-29.

Classification & Regulation

This clearance is catalogued under FDA product code IXI and 21 CFR 892.5710, within the Radiology review panel as a Class II device.