FDA 510(k)

Prospera Spectruum 負壓創傷治療黑色泡沫套件及白色泡沫配件

K 號：K250586 · 2025-11-21

決定日期2025-11-21

產品代碼OMP

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

Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 2025-11-21 under 510(k) number K250586. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory?

Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory is a medical device that received FDA 510(k) clearance on 2025-11-21. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K250586.

When did Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory receive FDA 510(k) clearance?

Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory received FDA 510(k) clearance on 2025-11-21, under 510(k) number K250586.

Who is the listed applicant for Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory?

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

What is the FDA product code for Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory?

The FDA product code for Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory is OMP.

其他以 Deroyal Industries, Inc. 為申請人之記錄

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。

K230233Prospera Spectruum 負壓創傷治療系統 K200631德瑞爾氏溫度監測探針 K200757福利氏導尿管配溫度感測器 K200319HYDRO-TEMP 新生兒皮膚表面溫度感測器，HYDRO-TEMP 新生兒皮膚表面溫度感測器配接線 K193027食道聽診器 9 法寸，食道聽診器 12 法寸，食道聽診器 18 法寸，食道聽診器，24 法寸 K191425水溫-溫度新生兒皮膚溫度探針蓋

查看所有 10 項裝置 →

相關器械（代碼：OMP）

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。

K261338RENASYS DYNAFLOW 套件（66807741）Smith & Nephew Medical, Ltd.K253263ConvaVAC™ 負壓傷口治療系統Convatec Limited, Gdc Building K253199CURASYS 2 (EMDN0003)CG Bio Co., Ltd.K260646RENASYS EDGE (66803126)Smith & Nephew Medical, Ltd.K261291Nisus NPWT 內容器 500-mL (CPC-500)Cork Medical K254019傷口基因NPWT系統Bechtel Medical, Inc.

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。