PULMONARY MONITOR— 510(k) K781922

Substantially Equivalent

Vitalograph , Ltd.

FDA 510(k) clearance K781922 for PULMONARY MONITOR, Substantially Equivalent on 1979-02-13. Applicant: Vitalograph , Ltd.. Device class: 2.

Clearance details

Applicant: Vitalograph , Ltd.
Product code: Code BZH
Device class: Class 2
Regulation: 21 CFR 868.1860
Advisory panel: Anesthesiology
Date received: 1978-11-13
Decision date: 1979-02-13
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.