meddevicedb.com FDA Device Reference

PANORAMA ENHANCEMENTS

K024042 Class II Traditional
Decision Date
2003-02-04
Sponsor / Applicant
Philips Medical Systems, Inc.

Technical Specification

510(k) Submission ID K024042
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2003-02-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PANORAMA ENHANCEMENTS received FDA 510(k) clearance under submission number K024042, sponsored by Philips Medical Systems, 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 2003-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.