3M Bair Hugger Universal Warming Gown made with Thinsulate Insulation

FDA 510(k) K210605 · 3M Company

Substantially Equivalent

510(k) numberK210605

Submission

Device name
3M Bair Hugger Universal Warming Gown made with Thinsulate Insulation
Applicant
3M Company
Saint Paul, MN, US
Received
March 1, 2021
Decision date
April 29, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DWJ – System, Thermal Regulating
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5900
Specialty
Cardiovascular

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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Questions and answers

When was 3M Bair Hugger Universal Warming Gown made with Thinsulate Insulation cleared by the FDA?

3M Bair Hugger Universal Warming Gown made with Thinsulate Insulation (K210605) received a 510(k) decision of Substantially Equivalent on April 29, 2021, 59 days after the submission was received.

What is the product code of K210605?

The FDA product code is DWJ – System, Thermal Regulating, a Class II (moderate risk) device regulated under 21 CFR 870.5900.