VITALOGRAPH-BREATHCO MONITOR— 510(k) K892524

Name: FDA 510(k) clearance K892524
Creator: U.S. Food and Drug Administration
Published: 1989-05-05

Substantially Equivalent

Vitalograph , Ltd.

FDA 510(k) clearance K892524 for VITALOGRAPH-BREATHCO MONITOR, Substantially Equivalent on 1989-05-05. Applicant: Vitalograph , Ltd.. Device class: 2.

Clearance details

Applicant: Vitalograph , Ltd.
Product code: Code CCJ
Device class: Class 2
Regulation: 21 CFR 868.1430
Advisory panel: Anesthesiology
Date received: 1989-04-11
Decision date: 1989-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

Download summary PDF View on FDA.gov ↗

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