VITALOGRAPH SPIROTRAC III— 510(k) K912412

Substantially Equivalent

Vitalograph , Ltd.

FDA 510(k) clearance K912412 for VITALOGRAPH SPIROTRAC III, Substantially Equivalent on 1991-10-15. Applicant: Vitalograph , Ltd.. Device class: 2.

Clearance details

Applicant: Vitalograph , Ltd.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1991-05-31
Decision date: 1991-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, 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.