°M Warmer System— 510(k) K232107

Name: FDA 510(k) clearance K232107
Creator: U.S. Food and Drug Administration
Published: 2024-05-31

Substantially Equivalent

Mequ A/S

FDA 510(k) clearance K232107 for °M Warmer System, Substantially Equivalent on 2024-05-31. Applicant: Mequ A/S. Device class: 2.

Clearance details

Applicant: Mequ A/S
Product code: Code LGZ
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 2023-07-14
Decision date: 2024-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kobenhavn N, DK

Download summary PDF View on FDA.gov ↗

Recent devices under product code LGZ

view all

K260988 — °M Warmer System with °M Station2026-04-24
K252636 — Fluido Compact System2025-11-18
K251733 — Fluido® AirGuard System2025-09-04
K211618 — Fluido Compact Blood and Fluid Warming System2023-06-05
K211800 — Warrior Blood and Fluid Warmer, Warrior EXTREME Blood and Fluid Warmer, Warrior Lite Blood and Fluid Warmer2022-12-08

Adverse events under product code LGZ

product code LGZ

Death: 16
Malfunction: 5,916
Other: 1
Total: 5,933

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.