MICRO MIST(TM) NEBULIZER
K-Number: K930525 · 1993-09-29
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Device Summary
Frequently Asked Questions
What is the MICRO MIST(TM) NEBULIZER?
MICRO MIST(TM) NEBULIZER is a medical device that received FDA 510(k) clearance on 1993-09-29. The listed applicant is Hudson Respiratory Care, Inc.. The 510(k) number is K930525.
When did MICRO MIST(TM) NEBULIZER receive FDA 510(k) clearance?
MICRO MIST(TM) NEBULIZER received FDA 510(k) clearance on 1993-09-29, under 510(k) number K930525.
Who is the listed applicant for MICRO MIST(TM) NEBULIZER?
The FDA 510(k) record lists Hudson Respiratory Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO MIST(TM) NEBULIZER?
The FDA product code for MICRO MIST(TM) 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 Hudson Respiratory Care, 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: 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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