meddevicedb.com FDA Device Reference

RADIONICS DISPOSABLE RF CANNULAE (SC-C, RFK-DB, RFK-DS)

K980430 Class II Traditional
Decision Date
1998-03-16
Sponsor / Applicant
Radionics, Inc.

Technical Specification

510(k) Submission ID K980430
Product Code GXI
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4725
Decision Date 1998-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIONICS DISPOSABLE RF CANNULAE (SC-C, RFK-DB, RFK-DS) received FDA 510(k) clearance under submission number K980430, 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 1998-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code GXI and 21 CFR 882.4725, within the Neurology review panel as a Class II device.