PULMONARY LAB AUTOMATION SYSTEM— 510(k) K801496

Name: FDA 510(k) clearance K801496
Creator: U.S. Food and Drug Administration
Published: 1980-07-21

Substantially Equivalent

Medical Graphics Corp.

FDA 510(k) clearance K801496 for PULMONARY LAB AUTOMATION SYSTEM, Substantially Equivalent on 1980-07-21. Applicant: Medical Graphics Corp.. Device class: 2.

Clearance details

Applicant: Medical Graphics Corp.
Product code: Code BZM
Device class: Class 2
Regulation: 21 CFR 868.1900
Advisory panel: Anesthesiology
Date received: 1980-06-26
Decision date: 1980-07-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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