EmoLED (v. 2-USA)
K 號：K240132 · 2024-03-12
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器材摘要
EmoLED (v. 2-USA) is the device name listed in this FDA 510(k) record. The listed applicant is Emoled, Srl. It received FDA 510(k) clearance on 2024-03-12 under 510(k) number K240132. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常見問題
What is the EmoLED (v. 2-USA)?
EmoLED (v. 2-USA) is a medical device that received FDA 510(k) clearance on 2024-03-12. The listed applicant is Emoled, Srl. The 510(k) number is K240132.
When did EmoLED (v. 2-USA) receive FDA 510(k) clearance?
EmoLED (v. 2-USA) received FDA 510(k) clearance on 2024-03-12, under 510(k) number K240132.
Who is the listed applicant for EmoLED (v. 2-USA)?
The FDA 510(k) record lists Emoled, Srl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EmoLED (v. 2-USA)?
The FDA product code for EmoLED (v. 2-USA) is GEX. This falls under the Gastroenterology category.
相關臨床試驗
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相關器械（代碼：GEX）
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。
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官方來源
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