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MONITORING STATION, CONNEX(R) CENTRAL STATION (CS)

K132807 Class II Special
Decision Date
2014-01-31
Sponsor / Applicant
Welch Allyn, Inc.

Technical Specification

510(k) Submission ID K132807
Product Code MWI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2014-01-31
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MONITORING STATION, CONNEX(R) CENTRAL STATION (CS) received FDA 510(k) clearance under submission number K132807, sponsored by Welch Allyn, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-01-31.

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.