SIDESTREAM DRUG NEBULIZER
K-Number: K914152 · 1992-05-05
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Device Summary
Frequently Asked Questions
What is the SIDESTREAM DRUG NEBULIZER?
SIDESTREAM DRUG NEBULIZER is a medical device that received FDA 510(k) clearance on 1992-05-05. The listed applicant is Medic-Aid , Ltd.. The 510(k) number is K914152.
When did SIDESTREAM DRUG NEBULIZER receive FDA 510(k) clearance?
SIDESTREAM DRUG NEBULIZER received FDA 510(k) clearance on 1992-05-05, under 510(k) number K914152.
Who is the listed applicant for SIDESTREAM DRUG NEBULIZER?
The FDA 510(k) record lists Medic-Aid , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIDESTREAM DRUG NEBULIZER?
The FDA product code for SIDESTREAM DRUG NEBULIZER is CAF.
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 Medic-Aid , Ltd. 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: CAF)
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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