meddevicedb.com FDA Device Reference

PROTON BEAM THERAPY SYSTEM (PBTS)

K992414 Class II Traditional
Decision Date
2000-07-21
Sponsor / Applicant
Optivus Technology, Inc.

Technical Specification

510(k) Submission ID K992414
Product Code LHN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2000-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROTON BEAM THERAPY SYSTEM (PBTS) received FDA 510(k) clearance under submission number K992414, sponsored by Optivus Technology, 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 2000-07-21.

Classification & Regulation

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