510(k) K231211

Device
Medline ComfortTemp Patient Warming System
Applicant
Medline Industries, LP
510(k) number
K231211
Product code
DWJ
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-01
Date received
2023-04-28
Regulation
870.5900
Classification name
System, Thermal Regulating
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Claire Pigman
Address
3 Lakes Dr. Northfield IL US 60093 60093

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
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20197344012838MEDLINEMEDLINE INDUSTRIES, INC.2024-06-25
20197344012814MEDLINEMEDLINE INDUSTRIES, INC.2024-06-25
20197344012777MEDLINEMEDLINE INDUSTRIES, INC.2024-06-25
20193489134794MEDLINEMEDLINE INDUSTRIES, INC.2024-06-25
20193489134787MEDLINEMEDLINE INDUSTRIES, INC.2024-06-25
20193489134770MEDLINEMEDLINE INDUSTRIES, INC.2024-06-25
20197344012791MedlineMEDLINE INDUSTRIES, INC.2024-04-30
10193489084917MedlineMEDLINE INDUSTRIES, INC.2024-03-25

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