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UNIPOLAR PEDIATRIC TEMPORARY PACING LEAD MOD. 6491

K922268 Class II Traditional
Decision Date
1992-11-23
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K922268
Product Code LDF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1992-11-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIPOLAR PEDIATRIC TEMPORARY PACING LEAD MOD. 6491 received FDA 510(k) clearance under submission number K922268, 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 1992-11-23.

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.