Calibration Gas for Carbon Dioxide Monitor

FDA 510(k) K874297 · Liquid Air Corp.

Substantially Equivalent

510(k) numberK874297

Submission

Device name
Calibration Gas for Carbon Dioxide Monitor
Applicant
Liquid Air Corp.
Walnut Creek, CA, US
Received
October 20, 1987
Decision date
December 21, 1987
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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K954804Lung Diffusion MixturesBXK · Traditional Mittler Supply, Inc.01/25/1996SE
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K954542Lung Diffusion MixtureBXK · Traditional Liquid Technology Corp.12/22/1995SE
K952838Medical Mixture-Lung Diffusion Gas MixturesBXK · Traditional Standard Welders Supply Co.09/19/1995SE
K953934Med-Tech Lung Diffusion MixtureBXK · Traditional Medical Technical Gases Inc..09/18/1995SE
K953208Medical Mixture-Clinical Blood Gas MixturesBXK · Traditional Standard Welders Supply Co.07/20/1995SE
K944998Calibration GasBXK · Traditional Sunox, Inc.02/03/1995SE
K944812Clinical Blood Gas MixtureBXK · Traditional Laboratory & Specialty Gases, Inc.02/01/1995SE
K942866Clinical Blood Gas MixtureBXK · Traditional Nordan Smith Welding Supplies09/01/1994SE
K932874Blood Gas MixtureBXK · Traditional Tri-Gas, Inc.01/27/1994SE

More from Tri-Gas, Inc.

510(k)DeviceDecision
K902754Anesthetic Gas Calibration MixtureBXK · Traditional 12/19/1990SE

Questions and answers

When was Calibration Gas for Carbon Dioxide Monitor cleared by the FDA?

Calibration Gas for Carbon Dioxide Monitor (K874297) received a 510(k) decision of Substantially Equivalent on December 21, 1987, 62 days after the submission was received.

What is the product code of K874297?

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