meddevicedb.com FDA Device Reference

RESPONSE ELECTROPHYSIOLOGY CATHETERS WITH LUMEN

K120544 Class II Special
Decision Date
2012-03-19
Sponsor / Applicant
St Jude Medical

Technical Specification

510(k) Submission ID K120544
Product Code DRF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1220
Decision Date 2012-03-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESPONSE ELECTROPHYSIOLOGY CATHETERS WITH LUMEN received FDA 510(k) clearance under submission number K120544, sponsored by St Jude Medical. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-03-19.

Classification & Regulation

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