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FDA 510(k)

CALIBRATION GAS FOR CARBON DIOXIDE MONITOR

K-Number: K874297 · 1987-12-21

Decision Date1987-12-21
Product CodeBXK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CALIBRATION GAS FOR CARBON DIOXIDE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Liquid Air Corp.. It received FDA 510(k) clearance on 1987-12-21 under 510(k) number K874297. The device is classified under product code BXK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALIBRATION GAS FOR CARBON DIOXIDE MONITOR?

CALIBRATION GAS FOR CARBON DIOXIDE MONITOR is a medical device that received FDA 510(k) clearance on 1987-12-21. The listed applicant is Liquid Air Corp.. The 510(k) number is K874297.

When did CALIBRATION GAS FOR CARBON DIOXIDE MONITOR receive FDA 510(k) clearance?

CALIBRATION GAS FOR CARBON DIOXIDE MONITOR received FDA 510(k) clearance on 1987-12-21, under 510(k) number K874297.

Who is the listed applicant for CALIBRATION GAS FOR CARBON DIOXIDE MONITOR?

The FDA 510(k) record lists Liquid Air Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CALIBRATION GAS FOR CARBON DIOXIDE MONITOR?

The FDA product code for CALIBRATION GAS FOR CARBON DIOXIDE MONITOR is BXK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Liquid Air Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: BXK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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