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VITALCHECK BLOOD PRESSURE CUFF, MODEL ZVC4000 SERIES

K082630 Class II Abbreviated
Decision Date
2008-12-19
Sponsor / Applicant
Zefon Intl.

Technical Specification

510(k) Submission ID K082630
Product Code DXQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1120
Decision Date 2008-12-19
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITALCHECK BLOOD PRESSURE CUFF, MODEL ZVC4000 SERIES received FDA 510(k) clearance under submission number K082630, sponsored by Zefon Intl.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code DXQ and 21 CFR 870.1120, within the Cardiovascular review panel as a Class II device.