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FDA 510(k)

Vapotherm霧化器适配器AAA-2

K 號:K220869 · 2022-10-28

決定日期2022-10-28
產品代碼CAF
諮詢委員會AN
決定相當於

器材摘要

Vapotherm Aerosol Adapter AAA-2 is the device name listed in this FDA 510(k) record. The listed applicant is Vapotherm, Inc.. It received FDA 510(k) clearance on 2022-10-28 under 510(k) number K220869. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vapotherm Aerosol Adapter AAA-2?

Vapotherm Aerosol Adapter AAA-2 is a medical device that received FDA 510(k) clearance on 2022-10-28. The listed applicant is Vapotherm, Inc.. The 510(k) number is K220869.

When did Vapotherm Aerosol Adapter AAA-2 receive FDA 510(k) clearance?

Vapotherm Aerosol Adapter AAA-2 received FDA 510(k) clearance on 2022-10-28, under 510(k) number K220869.

Who is the listed applicant for Vapotherm Aerosol Adapter AAA-2?

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

What is the FDA product code for Vapotherm Aerosol Adapter AAA-2?

The FDA product code for Vapotherm Aerosol Adapter AAA-2 is CAF.

相關臨床試驗

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。

其他以 Vapotherm, Inc. 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:CAF)

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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