Tablegard Pressure Relieving Patient Warming Mattress, Model: TG 700 HT

FDA 510(k) K080763 · Talley Medical

Substantially Equivalent

510(k) numberK080763

Submission

Device name
Tablegard Pressure Relieving Patient Warming Mattress, Model: TG 700 HT
Applicant
Talley Medical
Lansing, MI, US
Received
March 18, 2008
Decision date
May 30, 2008
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 Tablegard Pressure Relieving Patient Warming Mattress, Model: TG 700 HT cleared by the FDA?

Tablegard Pressure Relieving Patient Warming Mattress, Model: TG 700 HT (K080763) received a 510(k) decision of Substantially Equivalent on May 30, 2008, 73 days after the submission was received.

What is the product code of K080763?

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