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UNIPOLAR TEMP. MYOCARDIAL HEART WIRE, MODEL 6490

K895789 Class II Traditional
Decision Date
1989-12-07
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K895789
Product Code LDF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1989-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIPOLAR TEMP. MYOCARDIAL HEART WIRE, MODEL 6490 received FDA 510(k) clearance under submission number K895789, 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 1989-12-07.

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.