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UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494

K954809 Class II Traditional
Decision Date
1995-12-13
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K954809
Product Code LDF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1995-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494 received FDA 510(k) clearance under submission number K954809, 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 1995-12-13.

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.