FDA PMA

刺激器、骨成長、非侵襲的

PMA番号：P790002 · 2023-10-26

申請者Ahp Eos Buyer, Inc.

決定日2023-10-26

PMA番号P790002

製品コードLOF

デバイスクラスクラス3

診療科U

諮問委員会医薬品機器規制テキストの翻訳は以下の通りです。 [原文] OR [翻訳] OR 注：原文が具体的な内容を含んでいないため、翻訳は単なる「OR」のままです。

医療機器の概要

Stimulator, bone growth, non-invasive is the device name listed in this FDA 510(k) record. The listed applicant is Ahp Eos Buyer, Inc.. It received FDA 510(k) clearance on 2023-10-26. The device is classified under product code LOF. It was reviewed by the OR advisory panel.

よくある質問

What is the Stimulator, bone growth, non-invasive?

Stimulator, bone growth, non-invasive is a medical device that received FDA 510(k) clearance on 2023-10-26. The listed applicant is Ahp Eos Buyer, Inc..

When did Stimulator, bone growth, non-invasive receive FDA 510(k) clearance?

The clearance date for Stimulator, bone growth, non-invasive can be found in the official FDA records.

Who is the listed applicant for Stimulator, bone growth, non-invasive?

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

What is the FDA product code for Stimulator, bone growth, non-invasive?

The FDA product code for Stimulator, bone growth, non-invasive is LOF.

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医療機器の概要

よくある質問

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