VIRALIZER NEBULIZER SPRAYER— 510(k) K833474

Name: FDA 510(k) clearance K833474
Creator: U.S. Food and Drug Administration
Published: 1983-12-27

Substantially Equivalent

Viral Response System, Inc.

FDA 510(k) clearance K833474 for VIRALIZER NEBULIZER SPRAYER, Substantially Equivalent on 1983-12-27. Applicant: Viral Response System, Inc.. Device class: 1.

Clearance details

Applicant: Viral Response System, Inc.
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1983-10-06
Decision date: 1983-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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