FDA 510(k)

神經鎮痛器

K 號：K250818 · 2025-08-15

申請人Smart Alfa Teknoloji San. Ve Tic. A.S.

決定日期2025-08-15

產品代碼QRG

諮詢委員會AN

決定相當於

器材摘要

Nerveblox is the device name listed in this FDA 510(k) record. The listed applicant is Smart Alfa Teknoloji San. Ve Tic. A.S.. It received FDA 510(k) clearance on 2025-08-15 under 510(k) number K250818. The device is classified under product code QRG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Nerveblox?

Nerveblox is a medical device that received FDA 510(k) clearance on 2025-08-15. The listed applicant is Smart Alfa Teknoloji San. Ve Tic. A.S.. The 510(k) number is K250818.

When did Nerveblox receive FDA 510(k) clearance?

Nerveblox received FDA 510(k) clearance on 2025-08-15, under 510(k) number K250818.

Who is the listed applicant for Nerveblox?

The FDA 510(k) record lists Smart Alfa Teknoloji San. Ve Tic. A.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nerveblox?

The FDA product code for Nerveblox is QRG.

其他以 Smart Alfa Teknoloji San. Ve Tic. A.S. 為申請人之記錄

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相關器械（代碼：QRG）

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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