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VITAL SIGNS MONITOR-VSM 6000 SERIES

K101445 Class II Abbreviated
Decision Date
2010-06-08
Sponsor / Applicant
Welch Allyn, Inc.

Technical Specification

510(k) Submission ID K101445
Product Code MWI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2010-06-08
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITAL SIGNS MONITOR-VSM 6000 SERIES received FDA 510(k) clearance under submission number K101445, sponsored by Welch Allyn, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-06-08.

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.