Cocoon Convective Warming System, Model CWS7000

FDA 510(k) K232502 · Care Essentials Pty, Ltd.

Substantially Equivalent

510(k) numberK232502

Submission

Device name
Cocoon Convective Warming System, Model CWS7000
Applicant
Care Essentials Pty, Ltd.
North Geelong, AU
Received
August 18, 2023
Decision date
February 21, 2024
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 Cocoon Convective Warming System, Model CWS7000 cleared by the FDA?

Cocoon Convective Warming System, Model CWS7000 (K232502) received a 510(k) decision of Substantially Equivalent on February 21, 2024, 187 days after the submission was received.

What is the product code of K232502?

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