Anesthetic Gas Calibration Mixture

FDA 510(k) K902754 · Liquid Air Corp.

Substantially Equivalent

510(k) numberK902754

Submission

Device name
Anesthetic Gas Calibration Mixture
Applicant
Liquid Air Corp.
Washington, DC, US
Received
June 22, 1990
Decision date
December 19, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BXK – Gas, Calibration (Specified Concentration)
Device class
Class I (low risk)
Regulation
21 CFR 868.6400
Specialty
Anesthesiology

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More from Tri-Gas, Inc.

510(k)DeviceDecision
K874297Calibration Gas for Carbon Dioxide MonitorBXK · Traditional 12/21/1987SE

Questions and answers

When was Anesthetic Gas Calibration Mixture cleared by the FDA?

Anesthetic Gas Calibration Mixture (K902754) received a 510(k) decision of Substantially Equivalent on December 19, 1990, 180 days after the submission was received.

What is the product code of K902754?

The FDA product code is BXK – Gas, Calibration (Specified Concentration), a Class I (low risk) device regulated under 21 CFR 868.6400.