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FDA 510(k)

KLS Martin 口腔-馬克斯植入物 MR條件性(組合式)

K 號:K241314 · 2024-08-16

決定日期2024-08-16
產品代碼JEY
諮詢委員會DE
決定相當於

器材摘要

KLS Martin Oral-Max Implants MR Conditional (bundled) is the device name listed in this FDA 510(k) record. The listed applicant is KLS-Martin L.P.. It received FDA 510(k) clearance on 2024-08-16 under 510(k) number K241314. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the KLS Martin Oral-Max Implants MR Conditional (bundled)?

KLS Martin Oral-Max Implants MR Conditional (bundled) is a medical device that received FDA 510(k) clearance on 2024-08-16. The listed applicant is KLS-Martin L.P.. The 510(k) number is K241314.

When did KLS Martin Oral-Max Implants MR Conditional (bundled) receive FDA 510(k) clearance?

KLS Martin Oral-Max Implants MR Conditional (bundled) received FDA 510(k) clearance on 2024-08-16, under 510(k) number K241314.

Who is the listed applicant for KLS Martin Oral-Max Implants MR Conditional (bundled)?

FDA 510(k) 記錄將KLS-Martin L.P.列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for KLS Martin Oral-Max Implants MR Conditional (bundled)?

The FDA product code for KLS Martin Oral-Max Implants MR Conditional (bundled) is JEY.

相關臨床試驗

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其他以 KLS-Martin L.P. 為申請人之記錄

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相關器械(代碼:JEY)

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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