FDA 510(k)

シェルパパック心臓輸送システムおよびシェルパパック腎臓輸送システム

K番号: K180194 · 2018-03-30

決定日2018-03-30

製品コードMSB

諮問委員会以下は、指定された医療機器規制テキストの日本語訳です。以下の医療機器規制テキストを日本語に翻訳してください。会社名、製品名、FDA、510(k)、PMA、NCT、PMID、識別子、およびURLを保護してください。ポリシー：medical-regulatory-v1 [原文] GU [翻訳] GU

決定大幅同等

医療機器の概要

SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System is the device name listed in this FDA 510(k) record. The listed applicant is Paragonix Technologies, Inc.. It received FDA 510(k) clearance on 2018-03-30 under 510(k) number K180194. The device is classified under product code MSB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System?

SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System is a medical device that received FDA 510(k) clearance on 2018-03-30. The listed applicant is Paragonix Technologies, Inc.. The 510(k) number is K180194.

When did SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System receive FDA 510(k) clearance?

SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System received FDA 510(k) clearance on 2018-03-30, under 510(k) number K180194.

Who is the listed applicant for SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System?

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

What is the FDA product code for SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System?

The FDA product code for SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System is MSB.

申請者としてParagonix Technologies, Inc.を記載するその他の記録

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公式ソース

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