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MODEL 6500 UNIPOLAR TEMORARY MYOCARDIAL PACING LEAD

K012452 Class II Special
Decision Date
2001-08-14
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K012452
Product Code LDF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 2001-08-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 6500 UNIPOLAR TEMORARY MYOCARDIAL PACING LEAD received FDA 510(k) clearance under submission number K012452, sponsored by Medtronic Vascular. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2001-08-14.

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.