FDA 510(k)

ラツ Neurostat RF ガジェット

K番号: K232632 · 2024-05-24

決定日2024-05-24

製品コードGXD

諮問委員会Please provide the source text to translate.

決定大幅同等

医療機器の概要

Racz Neurostat RF Generator is the device name listed in this FDA 510(k) record. The listed applicant is Epimed International. It received FDA 510(k) clearance on 2024-05-24 under 510(k) number K232632. The device is classified under product code GXD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Racz Neurostat RF Generator?

Racz Neurostat RF Generator is a medical device that received FDA 510(k) clearance on 2024-05-24. The listed applicant is Epimed International. The 510(k) number is K232632.

When did Racz Neurostat RF Generator receive FDA 510(k) clearance?

Racz Neurostat RF Generator received FDA 510(k) clearance on 2024-05-24, under 510(k) number K232632.

Who is the listed applicant for Racz Neurostat RF Generator?

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

What is the FDA product code for Racz Neurostat RF Generator?

The FDA product code for Racz Neurostat RF Generator is GXD.

公式ソース

FDAデータベースで見る →

データはFDA Open APIから取得しています。最新かつ権威ある情報については、常に公式レコードを参照してください。

ラツ Neurostat RF ガジェット

医療機器の概要

よくある質問

関連する臨床試験

関連機器（コード：GXD）

公式ソース