meddevicedb.com FDA Device Reference

WATCH PAT 100S

K042916 Class II Traditional
Decision Date
2004-12-29
Sponsor / Applicant
Itamar Medical

Technical Specification

510(k) Submission ID K042916
Product Code MNR
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.2375
Decision Date 2004-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WATCH PAT 100S received FDA 510(k) clearance under submission number K042916, sponsored by Itamar Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2004-12-29.

Classification & Regulation

This clearance is catalogued under FDA product code MNR and 21 CFR 868.2375, within the Anesthesiology review panel as a Class II device.