FDA 510(k)

AccurSound Electronic Stethoscope AS-101

K番号: K221805 · 2023-03-23

決定日2023-03-23

製品コードDQD

諮問委員会以下は、提供された医療機器規制テキストの日本語訳です。 --- **政策：medical-regulatory-v1** --- [ここに原文が記載されています] --- **会社名/製品名**：[ここに会社名または製品名が記載されています] **FDA**：食品医薬品局 **510(k)**：510(k)届出 **PMA**：プレマーケティング評価届出 **NCT**：臨床試験登録番号 **PMID**：PubMed ID **識別子**：[ここに識別子が記載されています] **URL**：[ここにURLが記載されています]

決定大幅同等

医療機器の概要

AccurSound Electronic Stethoscope AS-101 is the device name listed in this FDA 510(k) record. The listed applicant is Heroic Faith International , Ltd.. It received FDA 510(k) clearance on 2023-03-23 under 510(k) number K221805. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the AccurSound Electronic Stethoscope AS-101?

AccurSound Electronic Stethoscope AS-101 is a medical device that received FDA 510(k) clearance on 2023-03-23. The listed applicant is Heroic Faith International , Ltd.. The 510(k) number is K221805.

When did AccurSound Electronic Stethoscope AS-101 receive FDA 510(k) clearance?

AccurSound Electronic Stethoscope AS-101 received FDA 510(k) clearance on 2023-03-23, under 510(k) number K221805.

Who is the listed applicant for AccurSound Electronic Stethoscope AS-101?

The FDA 510(k) record lists Heroic Faith International , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AccurSound Electronic Stethoscope AS-101?

The FDA product code for AccurSound Electronic Stethoscope AS-101 is DQD.

申請者としてHeroic Faith International , Ltd.を記載するその他の記録

K242798Airmod K242971AccurSound Electronic Stethoscope (AS101)

公式ソース

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