meddevicedb.com FDA Device Reference

SPACELABS MULTI-PARAMETER MODULE

K103142 Class II Special
Decision Date
2011-03-03
Sponsor / Applicant
Spacelabs Healthcare, Inc.

Technical Specification

510(k) Submission ID K103142
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2011-03-03
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPACELABS MULTI-PARAMETER MODULE received FDA 510(k) clearance under submission number K103142, sponsored by Spacelabs Healthcare, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-03-03.

Classification & Regulation

This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.