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PERMANENT AND TEMP. PACEMAKER ELECTRODE & LEAD ADA

K895136 Class III Traditional
Decision Date
1990-02-08
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K895136
Product Code DTB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1990-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERMANENT AND TEMP. PACEMAKER ELECTRODE & LEAD ADA received FDA 510(k) clearance under submission number K895136, 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 1990-02-08.

Classification & Regulation

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