AEROSOL DELIVERY HOOD
K-Number: K882396 · 1988-08-01
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Device Summary
Frequently Asked Questions
What is the AEROSOL DELIVERY HOOD?
AEROSOL DELIVERY HOOD is a medical device that received FDA 510(k) clearance on 1988-08-01. The listed applicant is Viratek, Inc.. The 510(k) number is K882396.
When did AEROSOL DELIVERY HOOD receive FDA 510(k) clearance?
AEROSOL DELIVERY HOOD received FDA 510(k) clearance on 1988-08-01, under 510(k) number K882396.
Who is the listed applicant for AEROSOL DELIVERY HOOD?
The FDA 510(k) record lists Viratek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AEROSOL DELIVERY HOOD?
The FDA product code for AEROSOL DELIVERY HOOD is BYL.
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.
Other records listing Viratek, Inc. as applicant
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: BYL)
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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