橫隔膜/肋間神經腹腔內植入刺激器
PMA 核准號：P200018 · 2023-03-31
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器材摘要
diaphragmatic/phrenic nerve laparoscopically-implanted stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Synapse Biomedical, Inc.. It received FDA 510(k) clearance on 2023-03-31. The device is classified under product code OIR. It was reviewed by the AN advisory panel.
常見問題
What is the diaphragmatic/phrenic nerve laparoscopically-implanted stimulator?
diaphragmatic/phrenic nerve laparoscopically-implanted stimulator is a medical device that received FDA 510(k) clearance on 2023-03-31. The listed applicant is Synapse Biomedical, Inc..
When did diaphragmatic/phrenic nerve laparoscopically-implanted stimulator receive FDA 510(k) clearance?
The clearance date for diaphragmatic/phrenic nerve laparoscopically-implanted stimulator can be found in the official FDA records.
Who is the listed applicant for diaphragmatic/phrenic nerve laparoscopically-implanted stimulator?
The FDA 510(k) record lists Synapse Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for diaphragmatic/phrenic nerve laparoscopically-implanted stimulator?
The FDA product code for diaphragmatic/phrenic nerve laparoscopically-implanted stimulator is OIR.
相關臨床試驗
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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