meddevicedb.com FDA Device Reference

RADIOACTIVE IODINE-125 SOURCES

K912170 Class II Traditional
Decision Date
1991-08-09
Sponsor / Applicant
Best Industries

Technical Specification

510(k) Submission ID K912170
Product Code IWI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5730
Decision Date 1991-08-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIOACTIVE IODINE-125 SOURCES received FDA 510(k) clearance under submission number K912170, sponsored by Best Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1991-08-09.

Classification & Regulation

This clearance is catalogued under FDA product code IWI and 21 CFR 892.5730, within the Radiology review panel as a Class II device.