meddevicedb.com FDA Device Reference

PROSTATE STEPPER TEMPLATE SET, MODEL PART NUMBER 189,065,189,066,189,067

K003270 Class II Special
Decision Date
2000-12-22
Sponsor / Applicant
Nucletron Corp.

Technical Specification

510(k) Submission ID K003270
Product Code JAQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5700
Decision Date 2000-12-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROSTATE STEPPER TEMPLATE SET, MODEL PART NUMBER 189,065,189,066,189,067 received FDA 510(k) clearance under submission number K003270, sponsored by Nucletron Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code JAQ and 21 CFR 892.5700, within the Radiology review panel as a Class II device.