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RADIONICS XDC EXTERNAL VENTRICULAR CATHETER

K992379 Class II Traditional
Decision Date
1999-09-08
Sponsor / Applicant
Radionics, Inc.

Technical Specification

510(k) Submission ID K992379
Product Code JXG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5550
Decision Date 1999-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIONICS XDC EXTERNAL VENTRICULAR CATHETER received FDA 510(k) clearance under submission number K992379, sponsored by Radionics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1999-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code JXG and 21 CFR 882.5550, within the Neurology review panel as a Class II device.