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Full Automatic (NIBP) Blood Pressure Monitor

K160557 Class II Traditional
Decision Date
2016-07-06
Sponsor / Applicant
Health & Life Co., Ltd.

Technical Specification

510(k) Submission ID K160557
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2016-07-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Full Automatic (NIBP) Blood Pressure Monitor received FDA 510(k) clearance under submission number K160557, sponsored by Health & Life Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-07-06.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.