MICROAIRE MODEL 2600
K-Number: K915670 · 1992-03-18
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Device Summary
Frequently Asked Questions
What is the MICROAIRE MODEL 2600?
MICROAIRE MODEL 2600 is a medical device that received FDA 510(k) clearance on 1992-03-18. The listed applicant is Microaire. The 510(k) number is K915670.
When did MICROAIRE MODEL 2600 receive FDA 510(k) clearance?
MICROAIRE MODEL 2600 received FDA 510(k) clearance on 1992-03-18, under 510(k) number K915670.
Who is the listed applicant for MICROAIRE MODEL 2600?
The FDA 510(k) record lists Microaire as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROAIRE MODEL 2600?
The FDA product code for MICROAIRE MODEL 2600 is GEF.
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 Microaire 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: GEF)
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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