LUNG DIFFUSION MIXTURE
K-Number: K954542 · 1995-12-22
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Device Summary
Frequently Asked Questions
What is the LUNG DIFFUSION MIXTURE?
LUNG DIFFUSION MIXTURE is a medical device that received FDA 510(k) clearance on 1995-12-22. The listed applicant is Liquid Technology Corp.. The 510(k) number is K954542.
When did LUNG DIFFUSION MIXTURE receive FDA 510(k) clearance?
LUNG DIFFUSION MIXTURE received FDA 510(k) clearance on 1995-12-22, under 510(k) number K954542.
Who is the listed applicant for LUNG DIFFUSION MIXTURE?
The FDA 510(k) record lists Liquid Technology Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUNG DIFFUSION MIXTURE?
The FDA product code for LUNG DIFFUSION 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 Technology 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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