VITALOGRAPH FUNCTION ANALYZER— 510(k) K791503

Name: FDA 510(k) clearance K791503
Creator: U.S. Food and Drug Administration
Published: 1979-08-16

Substantially Equivalent

Vitalograph , Ltd.

FDA 510(k) clearance K791503 for VITALOGRAPH FUNCTION ANALYZER, Substantially Equivalent on 1979-08-16. Applicant: Vitalograph , Ltd.. Device class: 2.

Clearance details

Applicant: Vitalograph , Ltd.
Product code: Code BZC
Device class: Class 2
Regulation: 21 CFR 868.1880
Advisory panel: Anesthesiology
Date received: 1979-08-08
Decision date: 1979-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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