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FDA 510(k)

AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini)

K 號:K253244 · 2026-02-23

決定日期2026-02-23
產品代碼IZL
諮詢委員會RA
決定相當於

器材摘要

AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini) is the device name listed in this FDA 510(k) record. The listed applicant is Poskom Co., Ltd.. It received FDA 510(k) clearance on 2026-02-23 under 510(k) number K253244. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini)?

AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini) is a medical device that received FDA 510(k) clearance on 2026-02-23. The listed applicant is Poskom Co., Ltd.. The 510(k) number is K253244.

When did AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini) receive FDA 510(k) clearance?

AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini) received FDA 510(k) clearance on 2026-02-23, under 510(k) number K253244.

Who is the listed applicant for AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini)?

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

What is the FDA product code for AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini)?

The FDA product code for AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini) is IZL.

相關臨床試驗

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其他以 Poskom Co., Ltd. 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

相關器械(代碼:IZL)

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

官方來源

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