AIRFLOMETER— 510(k) K780894

Substantially Equivalent

Glaxo Australia Ply. , Ltd.

FDA 510(k) clearance K780894 for AIRFLOMETER, Substantially Equivalent on 1978-12-14. Applicant: Glaxo Australia Ply. , Ltd.. Device class: 2.

Clearance details

Applicant: Glaxo Australia Ply. , Ltd.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1978-05-26
Decision date: 1978-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.