Klimamed Thermal Mat & Controller 95 and 55 Watts

FDA 510(k) K011859 · Klimamed Technologie Medizingerate GmbH

Substantially Equivalent

510(k) numberK011859

Submission

Device name
Klimamed Thermal Mat & Controller 95 and 55 Watts
Applicant
Klimamed Technologie Medizingerate GmbH
Roseville, CA, US
Received
June 14, 2001
Decision date
May 1, 2002
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 Klimamed Thermal Mat & Controller 95 and 55 Watts cleared by the FDA?

Klimamed Thermal Mat & Controller 95 and 55 Watts (K011859) received a 510(k) decision of Substantially Equivalent on May 1, 2002, 321 days after the submission was received.

What is the product code of K011859?

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