meddevicedb.com FDA Device Reference

SPACELABS HEALTHCARE TELEMETRY RECEIVER

K141156 Class II Traditional
Decision Date
2014-09-09
Sponsor / Applicant
Spacelabs Healthcare

Technical Specification

510(k) Submission ID K141156
Product Code MHX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2014-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPACELABS HEALTHCARE TELEMETRY RECEIVER received FDA 510(k) clearance under submission number K141156, sponsored by Spacelabs Healthcare. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-09-09.

Classification & Regulation

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