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FDA 510(k)

AIR-N-GO

K-Number: K110379 · 2011-12-08

ApplicantSatelec
Decision Date2011-12-08
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AIR-N-GO is the device name listed in this FDA 510(k) record. The listed applicant is Satelec. It received FDA 510(k) clearance on 2011-12-08 under 510(k) number K110379. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIR-N-GO?

AIR-N-GO is a medical device that received FDA 510(k) clearance on 2011-12-08. The listed applicant is Satelec. The 510(k) number is K110379.

When did AIR-N-GO receive FDA 510(k) clearance?

AIR-N-GO received FDA 510(k) clearance on 2011-12-08, under 510(k) number K110379.

Who is the listed applicant for AIR-N-GO?

The FDA 510(k) record lists Satelec as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIR-N-GO?

The FDA product code for AIR-N-GO is EFB.

Other records listing Satelec 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.

View all 24 devices →

Related Devices (Code: EFB)

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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