meddevicedb.com FDA Device Reference

Model X-100C CO-Met™ Oximetry System

K160231 Class II Traditional
Decision Date
2016-12-23
Sponsor / Applicant
Nonin Medical, Inc.

Technical Specification

510(k) Submission ID K160231
Product Code DQA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2700
Decision Date 2016-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Model X-100C CO-Met™ Oximetry System received FDA 510(k) clearance under submission number K160231, sponsored by Nonin Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-12-23.

Classification & Regulation

This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.