Temperature Probe-TP450

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K952804 ↗

FDA Product Code

FMT

Device Class

Class II

Regulation

21 CFR Part 880.5130

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Quantum Edge Pediatric Defirbrillation Electrodes

  Class III

  FDA 510(k) K970391 Active Cleared 6 Mar 1997

• Temperature Probe-TP550

  Class II

  FDA 510(k) K952805 Active Cleared 4 Apr 1996

• Noah Monitoring Electrode System

  Class II

  FDA 510(k) K970125 Active Cleared 4 Mar 1997

• Temperature PROBE-TP650

  Class II

  FDA 510(k) K952807 Active Cleared 4 Apr 1996

• Disposable Hydrogel Defibrillation Electrode/Pad

  Class III

  FDA 510(k) K960329 Active Cleared 2 Jul 1996

• Temperature PROBE-TP350

  Class II

  FDA 510(k) K952803 Active Cleared 4 Apr 1996

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