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FDA 510(k)

AIRFLOMETER

K-Number: K780894 · 1978-12-14

ApplicantGlaxo Australia Ply. , Ltd.
Decision Date1978-12-14
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AIRFLOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Glaxo Australia Ply. , Ltd.. It received FDA 510(k) clearance on 1978-12-14 under 510(k) number K780894. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRFLOMETER?

AIRFLOMETER is a medical device that received FDA 510(k) clearance on 1978-12-14. The listed applicant is Glaxo Australia Ply. , Ltd.. The 510(k) number is K780894.

When did AIRFLOMETER receive FDA 510(k) clearance?

AIRFLOMETER received FDA 510(k) clearance on 1978-12-14, under 510(k) number K780894.

Who is the listed applicant for AIRFLOMETER?

The FDA 510(k) record lists Glaxo Australia Ply. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIRFLOMETER?

The FDA product code for AIRFLOMETER is BZG.

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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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