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FDA 510(k)

Bact-Trap 過濾器、Bact-Trap Mini、Bact-Trap Midi、Pharma Mini HME/過濾器、Bact-HME HME/過濾器和 Bact-HME Midi HME/過濾器

K 號:K202459 · 2021-09-26

決定日期2021-09-26
產品代碼CAH
諮詢委員會AN
決定相當於

器材摘要

Bact-Trap Filter, Bact-Trap Mini, Bact-Trap Midi, Pharma Mini HME/Filter, Bact-HME HME/Filter and Bact-HME Midi HME/Filter is the device name listed in this FDA 510(k) record. The listed applicant is Pharma System AB. It received FDA 510(k) clearance on 2021-09-26 under 510(k) number K202459. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Bact-Trap Filter, Bact-Trap Mini, Bact-Trap Midi, Pharma Mini HME/Filter, Bact-HME HME/Filter and Bact-HME Midi HME/Filter?

Bact-Trap Filter, Bact-Trap Mini, Bact-Trap Midi, Pharma Mini HME/Filter, Bact-HME HME/Filter and Bact-HME Midi HME/Filter is a medical device that received FDA 510(k) clearance on 2021-09-26. The listed applicant is Pharma System AB. The 510(k) number is K202459.

When did Bact-Trap Filter, Bact-Trap Mini, Bact-Trap Midi, Pharma Mini HME/Filter, Bact-HME HME/Filter and Bact-HME Midi HME/Filter receive FDA 510(k) clearance?

Bact-Trap Filter, Bact-Trap Mini, Bact-Trap Midi, Pharma Mini HME/Filter, Bact-HME HME/Filter and Bact-HME Midi HME/Filter received FDA 510(k) clearance on 2021-09-26, under 510(k) number K202459.

Who is the listed applicant for Bact-Trap Filter, Bact-Trap Mini, Bact-Trap Midi, Pharma Mini HME/Filter, Bact-HME HME/Filter and Bact-HME Midi HME/Filter?

The FDA 510(k) record lists Pharma System AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bact-Trap Filter, Bact-Trap Mini, Bact-Trap Midi, Pharma Mini HME/Filter, Bact-HME HME/Filter and Bact-HME Midi HME/Filter?

The FDA product code for Bact-Trap Filter, Bact-Trap Mini, Bact-Trap Midi, Pharma Mini HME/Filter, Bact-HME HME/Filter and Bact-HME Midi HME/Filter is CAH.

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。

相關器械(代碼:CAH)

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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