meddevicedb.com FDA Device Reference

Disposable Needle Guides and Grids

K223689 Class II Traditional
Decision Date
2023-08-02
Sponsor / Applicant
Advance Medical Designs, Inc.

Technical Specification

510(k) Submission ID K223689
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2023-08-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Needle Guides and Grids received FDA 510(k) clearance under submission number K223689, sponsored by Advance Medical Designs, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2023-08-02.

Classification & Regulation

This clearance is catalogued under FDA product code ITX and 21 CFR 892.1570, within the Radiology review panel as a Class II device.