Unique Temp Warming Blankets, Model 8001140XXX

FDA 510(k) K093244 · Geratherm Medical AG

Substantially Equivalent

510(k) numberK093244

Submission

Device name
Unique Temp Warming Blankets, Model 8001140XXX
Applicant
Geratherm Medical AG
Tuttlingen, Baden Wurttemberg, DE
Received
October 15, 2009
Decision date
October 19, 2010
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 Unique Temp Warming Blankets, Model 8001140XXX cleared by the FDA?

Unique Temp Warming Blankets, Model 8001140XXX (K093244) received a 510(k) decision of Substantially Equivalent on October 19, 2010, 369 days after the submission was received.

What is the product code of K093244?

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