meddevicedb.com FDA Device Reference

MODEL 5311B A-V PACING SYSTEM ANALYZER

K910595 Class II Traditional
Decision Date
1991-05-07
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K910595
Product Code DTC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3630
Decision Date 1991-05-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 5311B A-V PACING SYSTEM ANALYZER received FDA 510(k) clearance under submission number K910595, 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 1991-05-07.

Classification & Regulation

This clearance is catalogued under FDA product code DTC and 21 CFR 870.3630, within the Cardiovascular review panel as a Class II device.