510(k) K232107

Device
°M Warmer System
Applicant
Mequ A/S
510(k) number
K232107
Product code
LGZ
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-31
Date received
2023-07-14
Regulation
880.5725
Classification name
Warmer, Thermal, Infusion Fluid
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Ulrik Andersen
Address
Ole Maaloes Vej 3 Kobenhavn N DK 2200 2200

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code LGZ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K260988°M Warmer System with °M StationMequ A/S2026-04-24
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K213191S-LineBarkey GmbH & Co. KG2022-05-24
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K181775Quantum Blood and IV Fluid Infusion WarmerLife Warmer, Inc.2019-01-28
K180154QiF Blood and Fluid WarmerQuality IN Flow , Ltd.2018-04-27
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K150404QiF Blood and Fluid WarmerQuality IN Flow , Ltd.2016-06-23