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PMA 核准號：P150024 · 2020-04-24
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器材摘要
Aspiration therapy system is the device name listed in this FDA 510(k) record. The listed applicant is Aspire Bariatrics, Inc.. It received FDA 510(k) clearance on 2020-04-24. The device is classified under product code OYF. It was reviewed by the GU advisory panel.
常見問題
What is the Aspiration therapy system?
Aspiration therapy system is a medical device that received FDA 510(k) clearance on 2020-04-24. The listed applicant is Aspire Bariatrics, Inc..
When did Aspiration therapy system receive FDA 510(k) clearance?
The clearance date for Aspiration therapy system can be found in the official FDA records.
Who is the listed applicant for Aspiration therapy system?
The FDA 510(k) record lists Aspire Bariatrics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aspiration therapy system?
The FDA product code for Aspiration therapy system is OYF.
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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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