脳卒中リハビリテーションのための埋込型自律神経刺激器
PMA番号：P210007 · 2026-09-16
広告
医療機器の概要
Stimulator, autonomic nerve, implanted for stroke rehabilitation is the device name listed in this FDA 510(k) record. The listed applicant is Mobia Medical, Inc.. It received FDA 510(k) clearance on 2026-09-16. The device is classified under product code QPY. It was reviewed by the PM advisory panel.
よくある質問
What is the Stimulator, autonomic nerve, implanted for stroke rehabilitation?
Stimulator, autonomic nerve, implanted for stroke rehabilitation is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is Mobia Medical, Inc..
When did Stimulator, autonomic nerve, implanted for stroke rehabilitation receive FDA 510(k) clearance?
The clearance date for Stimulator, autonomic nerve, implanted for stroke rehabilitation can be found in the official FDA records.
Who is the listed applicant for Stimulator, autonomic nerve, implanted for stroke rehabilitation?
The FDA 510(k) record lists Mobia Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, autonomic nerve, implanted for stroke rehabilitation?
The FDA product code for Stimulator, autonomic nerve, implanted for stroke rehabilitation is QPY.
関連する臨床試験
関連レコードは、名称、製品コード、その他のメタデータを使用して自動的にマッチングされます。マッチは検証された臨床的、科学的、企業的、または規制上の関係を確立するものではありません。リンクされた公式情報源をご確認ください。
NCT07608549FLASH試験フェーズ1安全性研究NOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751膀胱癌を診断するための人工知能（AI）アシストドのUro-Camカテーテル評価システムNOT_YET_RECRUITING
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。
広告