meddevicedb.com FDA Device Reference

EMPIRE N BLOOD PRESSURE MANOMETERS

K002955 Class II Traditional
Decision Date
2000-12-21
Sponsor / Applicant
Rudolf Riester GmbH & Co. KG

Technical Specification

510(k) Submission ID K002955
Product Code DXQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1120
Decision Date 2000-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMPIRE N BLOOD PRESSURE MANOMETERS received FDA 510(k) clearance under submission number K002955, sponsored by Rudolf Riester GmbH & Co. KG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-12-21.

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.