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FDA 510(k)

PERF-GEN 閃脈灌注解決方案

K 號:K221386 · 2022-06-14

決定日期2022-06-14
產品代碼KDL
諮詢委員會GU
決定相當於

器材摘要

PERF-GEN Pulsatile Perfusion Solution is the device name listed in this FDA 510(k) record. The listed applicant is Institut Georges Lopez. It received FDA 510(k) clearance on 2022-06-14 under 510(k) number K221386. The device is classified under product code KDL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the PERF-GEN Pulsatile Perfusion Solution?

PERF-GEN Pulsatile Perfusion Solution is a medical device that received FDA 510(k) clearance on 2022-06-14. The listed applicant is Institut Georges Lopez. The 510(k) number is K221386.

When did PERF-GEN Pulsatile Perfusion Solution receive FDA 510(k) clearance?

PERF-GEN Pulsatile Perfusion Solution received FDA 510(k) clearance on 2022-06-14, under 510(k) number K221386.

Who is the listed applicant for PERF-GEN Pulsatile Perfusion Solution?

The FDA 510(k) record lists Institut Georges Lopez as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERF-GEN Pulsatile Perfusion Solution?

The FDA product code for PERF-GEN Pulsatile Perfusion Solution is KDL.

相關臨床試驗

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其他以 Institut Georges Lopez 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:KDL)

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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