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VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221

K051857 Class II Traditional
Decision Date
2005-09-15
Sponsor / Applicant
Weissburg Associates

Technical Specification

510(k) Submission ID K051857
Product Code CCK
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1400
Decision Date 2005-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221 received FDA 510(k) clearance under submission number K051857, sponsored by Weissburg Associates. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2005-09-15.

Classification & Regulation

This clearance is catalogued under FDA product code CCK and 21 CFR 868.1400, within the Anesthesiology review panel as a Class II device.