LUNG DIFFUSION MIXTURES
K-Number: K954804 · 1996-01-25
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Device Summary
Frequently Asked Questions
What is the LUNG DIFFUSION MIXTURES?
LUNG DIFFUSION MIXTURES is a medical device that received FDA 510(k) clearance on 1996-01-25. The listed applicant is Mittler Supply, Inc.. The 510(k) number is K954804.
When did LUNG DIFFUSION MIXTURES receive FDA 510(k) clearance?
LUNG DIFFUSION MIXTURES received FDA 510(k) clearance on 1996-01-25, under 510(k) number K954804.
Who is the listed applicant for LUNG DIFFUSION MIXTURES?
The FDA 510(k) record lists Mittler Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUNG DIFFUSION MIXTURES?
The FDA product code for LUNG DIFFUSION MIXTURES 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 Mittler Supply, Inc. 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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