meddevicedb.com FDA Device Reference

External Drainage System

K221694 Class II Traditional
Decision Date
2023-02-09
Sponsor / Applicant
Jmed(Shenzhen) Technology Limited

Technical Specification

510(k) Submission ID K221694
Product Code JXG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5550
Decision Date 2023-02-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

External Drainage System received FDA 510(k) clearance under submission number K221694, sponsored by Jmed(Shenzhen) Technology Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2023-02-09.

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.