TUBA TM (TRANSIT-TIME ULTRASONIC BREATH ANALYZER)— 510(k) K900331

Name: FDA 510(k) clearance K900331
Creator: U.S. Food and Drug Administration
Published: 1990-09-04

Substantially Equivalent

Ghg Medizin-Elektronik AG

FDA 510(k) clearance K900331 for TUBA TM (TRANSIT-TIME ULTRASONIC BREATH ANALYZER), Substantially Equivalent on 1990-09-04. Applicant: Ghg Medizin-Elektronik AG. Device class: 2.

Clearance details

Applicant: Ghg Medizin-Elektronik AG
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1990-01-23
Decision date: 1990-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Zurich Z H, CH

Download summary PDF View on FDA.gov ↗

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