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FDA 510(k)

FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)

K-Number: K260270 · 2026-06-02

ApplicantFindAir Sp. z o.o.
Decision Date2026-06-02
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FindAir ONE for pMDI (FAO-MDI-V12-GRE-001) is the device name listed in this FDA 510(k) record. The listed applicant is FindAir Sp. z o.o.. It received FDA 510(k) clearance on 2026-06-02 under 510(k) number K260270. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)?

FindAir ONE for pMDI (FAO-MDI-V12-GRE-001) is a medical device that received FDA 510(k) clearance on 2026-06-02. The listed applicant is FindAir Sp. z o.o.. The 510(k) number is K260270.

When did FindAir ONE for pMDI (FAO-MDI-V12-GRE-001) receive FDA 510(k) clearance?

FindAir ONE for pMDI (FAO-MDI-V12-GRE-001) received FDA 510(k) clearance on 2026-06-02, under 510(k) number K260270.

Who is the listed applicant for FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)?

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

What is the FDA product code for FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)?

The FDA product code for FindAir ONE for pMDI (FAO-MDI-V12-GRE-001) is CAF.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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