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DETECT SURGICAL PACING AND MAPPING TOOL

K040812 Class II Traditional
Decision Date
2004-09-02
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K040812
Product Code LDF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 2004-09-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DETECT SURGICAL PACING AND MAPPING TOOL received FDA 510(k) clearance under submission number K040812, sponsored by Medtronic Vascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-09-02.

Classification & Regulation

This clearance is catalogued under FDA product code LDF and 21 CFR 870.3680, within the Cardiovascular review panel as a Class II device.