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CONNEX WORKSTATION

K120343 Class II Special
Decision Date
2012-02-24
Sponsor / Applicant
Welch Allyn, Inc.

Technical Specification

510(k) Submission ID K120343
Product Code MWI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2012-02-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONNEX WORKSTATION received FDA 510(k) clearance under submission number K120343, 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 2012-02-24.

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.