meddevicedb.com FDA Device Reference

Infinity Gateway Suite

K203579 Class II Traditional
Decision Date
2022-06-07
Sponsor / Applicant
Draeger Medical Systems, Inc.

Technical Specification

510(k) Submission ID K203579
Product Code MSX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2022-06-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Infinity Gateway Suite received FDA 510(k) clearance under submission number K203579, sponsored by Draeger Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2022-06-07.

Classification & Regulation

This clearance is catalogued under FDA product code MSX and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.