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SENSOMETRICS SOFTWARE

K101133 Class II Traditional
Decision Date
2010-11-18
Sponsor / Applicant
Dpcom AS

Technical Specification

510(k) Submission ID K101133
Product Code GWM
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1620
Decision Date 2010-11-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SENSOMETRICS SOFTWARE received FDA 510(k) clearance under submission number K101133, sponsored by Dpcom AS. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2010-11-18.

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.