FDA 510(k)

LiteAire基本雙閥可折疊MDI保持腔

K 號：K210558 · 2022-04-01

決定日期2022-04-01

產品代碼NVP

諮詢委員會AN

決定相當於

器材摘要

LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber is the device name listed in this FDA 510(k) record. The listed applicant is Thayer Medical Corporation. It received FDA 510(k) clearance on 2022-04-01 under 510(k) number K210558. The device is classified under product code NVP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber?

LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber is a medical device that received FDA 510(k) clearance on 2022-04-01. The listed applicant is Thayer Medical Corporation. The 510(k) number is K210558.

When did LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber receive FDA 510(k) clearance?

LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber received FDA 510(k) clearance on 2022-04-01, under 510(k) number K210558.

Who is the listed applicant for LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber?

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

What is the FDA product code for LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber?

The FDA product code for LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber is NVP.

其他以 Thayer Medical Corporation 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。

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相關器械（代碼：NVP）

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。

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官方來源

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