meddevicedb.com FDA Device Reference

CALYPSO 4D LOCALIZATION SYSTEM

K060906 Class II Traditional
Decision Date
2006-07-28
Sponsor / Applicant
Calypso Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K060906
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2006-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CALYPSO 4D LOCALIZATION SYSTEM received FDA 510(k) clearance under submission number K060906, sponsored by Calypso Medical Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-07-28.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.