meddevicedb.com FDA Device Reference

MODEL 9300 TREND ANALYZING BIO-MONITOR SYS

K844252 Class II Traditional
Decision Date
1985-06-26
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K844252
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 1985-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 9300 TREND ANALYZING BIO-MONITOR SYS received FDA 510(k) clearance under submission number K844252, 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 1985-06-26.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.