meddevicedb.com FDA Device Reference

ELECTROPHYSIOLOGY CATHETER

K030109 Class II Traditional
Decision Date
2003-08-08
Sponsor / Applicant
Alliance Medical Corp.

Technical Specification

510(k) Submission ID K030109
Product Code NLH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1220
Decision Date 2003-08-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTROPHYSIOLOGY CATHETER received FDA 510(k) clearance under submission number K030109, sponsored by Alliance Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-08-08.

Classification & Regulation

This clearance is catalogued under FDA product code NLH and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.