ANESTHETIC GAS CALIBRATION MIXTURE
K-Number: K902754 · 1990-12-19
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Device Summary
Frequently Asked Questions
What is the ANESTHETIC GAS CALIBRATION MIXTURE?
ANESTHETIC GAS CALIBRATION MIXTURE is a medical device that received FDA 510(k) clearance on 1990-12-19. The listed applicant is Liquid Air Corp.. The 510(k) number is K902754.
When did ANESTHETIC GAS CALIBRATION MIXTURE receive FDA 510(k) clearance?
ANESTHETIC GAS CALIBRATION MIXTURE received FDA 510(k) clearance on 1990-12-19, under 510(k) number K902754.
Who is the listed applicant for ANESTHETIC GAS CALIBRATION MIXTURE?
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 ANESTHETIC GAS CALIBRATION MIXTURE?
The FDA product code for ANESTHETIC GAS CALIBRATION MIXTURE 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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