3000 AEROSOL TWO
K-Number: K943990 · 1995-03-21
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Device Summary
Frequently Asked Questions
What is the 3000 AEROSOL TWO?
3000 AEROSOL TWO is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is Medical Industries America, Inc.. The 510(k) number is K943990.
When did 3000 AEROSOL TWO receive FDA 510(k) clearance?
3000 AEROSOL TWO received FDA 510(k) clearance on 1995-03-21, under 510(k) number K943990.
Who is the listed applicant for 3000 AEROSOL TWO?
The FDA 510(k) record lists Medical Industries America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 3000 AEROSOL TWO?
The FDA product code for 3000 AEROSOL TWO 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 Medical Industries America, 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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