meddevicedb.com FDA Device Reference

MENTOR ISOLOADER AUTOMATIC NEEDLE LOADING SYSTEM AND PHYSICS WORKSTATION FOR BRACHYTHERAPY

K011493 Class II Traditional
Decision Date
2002-10-01
Sponsor / Applicant
Mentor Corp.

Technical Specification

510(k) Submission ID K011493
Product Code KPT
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1360
Decision Date 2002-10-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MENTOR ISOLOADER AUTOMATIC NEEDLE LOADING SYSTEM AND PHYSICS WORKSTATION FOR BRACHYTHERAPY received FDA 510(k) clearance under submission number K011493, sponsored by Mentor Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code KPT and 21 CFR 892.1360, within the Radiology review panel as a Class II device.