meddevicedb.com FDA Device Reference

WVSM (WIRELESS VITAL SIGNS MONITOR), MODEL 5.0

K101674 Class II Traditional
Decision Date
2010-07-21
Sponsor / Applicant
Athena Gtx

Technical Specification

510(k) Submission ID K101674
Product Code MWI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2010-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WVSM (WIRELESS VITAL SIGNS MONITOR), MODEL 5.0 received FDA 510(k) clearance under submission number K101674, sponsored by Athena Gtx. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-07-21.

Classification & Regulation

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