Temp Marq(Tm) Convective Warming System

FDA 510(k) K904690 · Marquest Medical Products, Inc.

Substantially Equivalent

510(k) numberK904690

Submission

Device name
Temp Marq(Tm) Convective Warming System
Applicant
Marquest Medical Products, Inc.
Englewood, CO, US
Received
October 16, 1990
Decision date
February 1, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K961838Respirgard II, SpirogardCAH · Traditional 10/18/1996SE
K960972Disposable Gas Sampling Interface KitsCCK · Traditional 10/18/1996SE
K903138Marquest SCT 3000, Heated Humidification SystemBTT · Traditional 10/11/1990SE
K902632Gas-Lyte 1CC and 3CC Arterial Blood SamplersCBT · Traditional 09/04/1990SE
K903307Temp Marq Temperature Trend IndicatorKPD · Traditional 08/17/1990SE
K880979Marquest SCT 2000, Heated Humidification SystemBTT · Traditional 07/15/1988SE

Questions and answers

When was Temp Marq(Tm) Convective Warming System cleared by the FDA?

Temp Marq(Tm) Convective Warming System (K904690) received a 510(k) decision of Substantially Equivalent on February 1, 1991, 108 days after the submission was received.

What is the product code of K904690?

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