meddevicedb.com FDA Device Reference

SureSigns VS3, SureSigns VS4

K151761 Class II Special
Decision Date
2015-09-29
Sponsor / Applicant
Phillips Medical Systems

Technical Specification

510(k) Submission ID K151761
Product Code DSJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1100
Decision Date 2015-09-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SureSigns VS3, SureSigns VS4 received FDA 510(k) clearance under submission number K151761, sponsored by Phillips Medical Systems. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code DSJ and 21 CFR 870.1100, within the Cardiovascular review panel as a Class II device.