meddevicedb.com FDA Device Reference

NEUROTREND MULTIPARAMETER SENSOR, C7004S, TO OPERATE WITH PARATREND 7+ MULTIPARAMETER SENSOR, MPM7001S, AND SATELLITE MS

K980380 Class II Traditional
Decision Date
1999-07-14
Sponsor / Applicant
Diametrics Medical, Ltd.

Technical Specification

510(k) Submission ID K980380
Product Code GWM
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1620
Decision Date 1999-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROTREND MULTIPARAMETER SENSOR, C7004S, TO OPERATE WITH PARATREND 7+ MULTIPARAMETER SENSOR, MPM7001S, AND SATELLITE MS received FDA 510(k) clearance under submission number K980380, sponsored by Diametrics Medical, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1999-07-14.

Classification & Regulation

This clearance is catalogued under FDA product code GWM and 21 CFR 882.1620, within the Neurology review panel as a Class II device.