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APPLICATORS FOR AFTERLOADING BRACHYTHERAPY

K082530 Class II Abbreviated
Decision Date
2008-10-30
Sponsor / Applicant
Isodose Control B.V.

Technical Specification

510(k) Submission ID K082530
Product Code JAQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5700
Decision Date 2008-10-30
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APPLICATORS FOR AFTERLOADING BRACHYTHERAPY received FDA 510(k) clearance under submission number K082530, sponsored by Isodose Control B.V.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2008-10-30.

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.