meddevicedb.com FDA Device Reference

OMRON MODEL HBP-2070 VITAL SIGNS MONITOR

K082812 Class II Special
Decision Date
2008-10-22
Sponsor / Applicant
Omron Healthcare, Inc.

Technical Specification

510(k) Submission ID K082812
Product Code MWI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2008-10-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OMRON MODEL HBP-2070 VITAL SIGNS MONITOR received FDA 510(k) clearance under submission number K082812, sponsored by Omron Healthcare, 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 2008-10-22.

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.