meddevicedb.com FDA Device Reference

Thermogard HQ™ Temperature Management System, Thermogard XP® Temperature Management System (VitalTemp™ Universal Pad)

K250979 Class II Traditional
Decision Date
2025-10-15
Sponsor / Applicant
Zoll Circulation, Inc.

Technical Specification

510(k) Submission ID K250979
Product Code NZE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5900
Decision Date 2025-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Thermogard HQ™ Temperature Management System, Thermogard XP® Temperature Management System (VitalTemp™ Universal Pad) received FDA 510(k) clearance under submission number K250979, sponsored by Zoll Circulation, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2025-10-15.

Classification & Regulation

This clearance is catalogued under FDA product code NZE and 21 CFR 870.5900, within the Cardiovascular review panel as a Class II device.