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FDA 510(k)

收穫牙醫 HD 牙齦條

K 號:K231389 · 2023-08-16

決定日期2023-08-16
產品代碼EBI
諮詢委員會DE
決定相當於

器材摘要

Harvest Dental HD Gum Strip is the device name listed in this FDA 510(k) record. The listed applicant is Harvest Dental Products, LLC. It received FDA 510(k) clearance on 2023-08-16 under 510(k) number K231389. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Harvest Dental HD Gum Strip?

Harvest Dental HD Gum Strip is a medical device that received FDA 510(k) clearance on 2023-08-16. The listed applicant is Harvest Dental Products, LLC. The 510(k) number is K231389.

When did Harvest Dental HD Gum Strip receive FDA 510(k) clearance?

Harvest Dental HD Gum Strip received FDA 510(k) clearance on 2023-08-16, under 510(k) number K231389.

Who is the listed applicant for Harvest Dental HD Gum Strip?

The FDA 510(k) record lists Harvest Dental Products, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Harvest Dental HD Gum Strip?

The FDA product code for Harvest Dental HD Gum Strip is EBI.

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。

其他以 Harvest Dental Products, LLC 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。

相關器械(代碼:EBI)

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

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