meddevicedb.com FDA Device Reference

SURESIGNS VSI VITAL SIGNS MONITOR

K110803 Class II Traditional
Decision Date
2011-05-20
Sponsor / Applicant
Philips Medical Systems

Technical Specification

510(k) Submission ID K110803
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2011-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURESIGNS VSI VITAL SIGNS MONITOR received FDA 510(k) clearance under submission number K110803, sponsored by Philips Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-05-20.

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.