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FDA 510(k)

米達流量計;電子自動化測量系統

K 號:K241465 · 2024-09-19

決定日期2024-09-19
產品代碼BZR
諮詢委員會AN
決定相當於

器材摘要

Midas Flowmeter; eAVS is the device name listed in this FDA 510(k) record. The listed applicant is Parker Hannifin Corporation. It received FDA 510(k) clearance on 2024-09-19 under 510(k) number K241465. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Midas Flowmeter; eAVS?

Midas Flowmeter; eAVS is a medical device that received FDA 510(k) clearance on 2024-09-19. The listed applicant is Parker Hannifin Corporation. The 510(k) number is K241465.

When did Midas Flowmeter; eAVS receive FDA 510(k) clearance?

Midas Flowmeter; eAVS received FDA 510(k) clearance on 2024-09-19, under 510(k) number K241465.

Who is the listed applicant for Midas Flowmeter; eAVS?

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

What is the FDA product code for Midas Flowmeter; eAVS?

The FDA product code for Midas Flowmeter; eAVS is BZR.

相關臨床試驗

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其他以 Parker Hannifin Corporation 為申請人之記錄

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相關器械(代碼:BZR)

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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