免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

JRP 疤痕擴散器

K 號:K152538 · 2016-04-13

決定日期2016-04-13
產品代碼GAD
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

JRP Wound Spreader is the device name listed in this FDA 510(k) record. The listed applicant is J.R. Parker, LLC. It received FDA 510(k) clearance on 2016-04-13 under 510(k) number K152538. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the JRP Wound Spreader?

JRP Wound Spreader is a medical device that received FDA 510(k) clearance on 2016-04-13. The listed applicant is J.R. Parker, LLC. The 510(k) number is K152538.

When did JRP Wound Spreader receive FDA 510(k) clearance?

JRP Wound Spreader received FDA 510(k) clearance on 2016-04-13, under 510(k) number K152538.

Who is the listed applicant for JRP Wound Spreader?

The FDA 510(k) record lists J.R. Parker, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JRP Wound Spreader?

The FDA product code for JRP Wound Spreader is GAD.

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。

相關器械(代碼:GAD)

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。

↑