meddevicedb.com FDA Device Reference

PRE-WAXED NEEDLES WITH GOLD FIDUCIARY MARKERS

K071550 Class II Abbreviated
Decision Date
2007-07-18
Sponsor / Applicant
Cp Medical

Technical Specification

510(k) Submission ID K071550
Product Code KXK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5730
Decision Date 2007-07-18
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRE-WAXED NEEDLES WITH GOLD FIDUCIARY MARKERS received FDA 510(k) clearance under submission number K071550, sponsored by Cp Medical. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2007-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code KXK and 21 CFR 892.5730, within the Radiology review panel as a Class II device.