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MEDTRONIC MODEL 9410 TELETRACE RECEIVER

K791778 Class II Traditional
Decision Date
1979-10-02
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K791778
Product Code DXH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2920
Decision Date 1979-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDTRONIC MODEL 9410 TELETRACE RECEIVER received FDA 510(k) clearance under submission number K791778, 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 1979-10-02.

Classification & Regulation

This clearance is catalogued under FDA product code DXH and 21 CFR 870.2920, within the Cardiovascular review panel as a Class II device.