meddevicedb.com FDA Device Reference

MODIFICATION TO HEXAPOD RT COUCH TOP

K062639 Class II Special
Decision Date
2006-09-21
Sponsor / Applicant
Medical Intelligence Medizintechnik-GmbH-An Elekta

Technical Specification

510(k) Submission ID K062639
Product Code JAI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5770
Decision Date 2006-09-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO HEXAPOD RT COUCH TOP received FDA 510(k) clearance under submission number K062639, sponsored by Medical Intelligence Medizintechnik-GmbH-An Elekta. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-09-21.

Classification & Regulation

This clearance is catalogued under FDA product code JAI and 21 CFR 892.5770, within the Radiology review panel as a Class II device.