meddevicedb.com FDA Device Reference

NIRO-200NX DP

K162117 Class II Traditional
Decision Date
2016-10-25
Sponsor / Applicant
Hamamatsu Photonics K.K.

Technical Specification

510(k) Submission ID K162117
Product Code MUD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2700
Decision Date 2016-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NIRO-200NX DP received FDA 510(k) clearance under submission number K162117, sponsored by Hamamatsu Photonics K.K.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-10-25.

Classification & Regulation

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