meddevicedb.com FDA Device Reference

BLOOD PRESSURE METER, MODELS CH-631B, CH-631D, CH-632B, CH-632D

K001244 Class II Traditional
Decision Date
2000-09-26
Sponsor / Applicant
Citizen Watch Co., Ltd.

Technical Specification

510(k) Submission ID K001244
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2000-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD PRESSURE METER, MODELS CH-631B, CH-631D, CH-632B, CH-632D received FDA 510(k) clearance under submission number K001244, sponsored by Citizen Watch 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 2000-09-26.

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.