MICROAIR TURN-Q
K-Number: K926456 · 1993-03-24
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Device Summary
Frequently Asked Questions
What is the MICROAIR TURN-Q?
MICROAIR TURN-Q is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Gsi Development Co.. The 510(k) number is K926456.
When did MICROAIR TURN-Q receive FDA 510(k) clearance?
MICROAIR TURN-Q received FDA 510(k) clearance on 1993-03-24, under 510(k) number K926456.
Who is the listed applicant for MICROAIR TURN-Q?
The FDA 510(k) record lists Gsi Development Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROAIR TURN-Q?
The FDA product code for MICROAIR TURN-Q is IOQ.
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 Gsi Development Co. 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: IOQ)
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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