meddevicedb.com FDA Device Reference

VARIPLAN COMPUT. RADIOTHERAPY

K761265 Class II Traditional
Decision Date
1976-12-21
Sponsor / Applicant
Varian Assoc., Inc.

Technical Specification

510(k) Submission ID K761265
Product Code KPQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5840
Decision Date 1976-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VARIPLAN COMPUT. RADIOTHERAPY received FDA 510(k) clearance under submission number K761265, sponsored by Varian Assoc., 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 1976-12-21.

Classification & Regulation

This clearance is catalogued under FDA product code KPQ and 21 CFR 892.5840, within the Radiology review panel as a Class II device.