VMT HAND HELD NEBULIZER— 510(k) K841894

Name: FDA 510(k) clearance K841894
Creator: U.S. Food and Drug Administration
Published: 1984-06-05

Substantially Equivalent

Vortran Medical Technology 1, Inc.

FDA 510(k) clearance K841894 for VMT HAND HELD NEBULIZER, Substantially Equivalent on 1984-06-05. Applicant: Vortran Medical Technology 1, Inc.. Device class: 1.

Clearance details

Applicant: Vortran Medical Technology 1, Inc.
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1984-05-07
Decision date: 1984-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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