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FDA 510(k)

LUNG DIFFUSION

K-Number: K935309 · 1994-09-27

ApplicantAcetylene Gas Co.
Decision Date1994-09-27
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LUNG DIFFUSION is the device name listed in this FDA 510(k) record. The listed applicant is Acetylene Gas Co.. It received FDA 510(k) clearance on 1994-09-27 under 510(k) number K935309. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUNG DIFFUSION?

LUNG DIFFUSION is a medical device that received FDA 510(k) clearance on 1994-09-27. The listed applicant is Acetylene Gas Co.. The 510(k) number is K935309.

When did LUNG DIFFUSION receive FDA 510(k) clearance?

LUNG DIFFUSION received FDA 510(k) clearance on 1994-09-27, under 510(k) number K935309.

Who is the listed applicant for LUNG DIFFUSION?

The FDA 510(k) record lists Acetylene Gas Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LUNG DIFFUSION?

The FDA product code for LUNG DIFFUSION is BZC.

Related Clinical Trials

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Other records listing Acetylene Gas Co. 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.

K935310MEDICAL LASER MIXTUREK935311CLINICAL BLOOD GAS

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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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