VIRALIZER NEBULIZER SPRAYER
K-Number: K833474 · 1983-12-27
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Device Summary
Frequently Asked Questions
What is the VIRALIZER NEBULIZER SPRAYER?
VIRALIZER NEBULIZER SPRAYER is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Viral Response System, Inc.. The 510(k) number is K833474.
When did VIRALIZER NEBULIZER SPRAYER receive FDA 510(k) clearance?
VIRALIZER NEBULIZER SPRAYER received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833474.
Who is the listed applicant for VIRALIZER NEBULIZER SPRAYER?
The FDA 510(k) record lists Viral Response System, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIRALIZER NEBULIZER SPRAYER?
The FDA product code for VIRALIZER NEBULIZER SPRAYER is CCQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CCQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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