meddevicedb.com FDA Device Reference

eCareManager 4.0.1

K153156 Class II Traditional
Decision Date
2016-09-30
Sponsor / Applicant
Visicu, Inc.

Technical Specification

510(k) Submission ID K153156
Product Code MSX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2016-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

eCareManager 4.0.1 received FDA 510(k) clearance under submission number K153156, sponsored by Visicu, 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 2016-09-30.

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.