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FDA 510(k)

攜帶式牙科X光機(NR-F350、CS 2400P、CS 2300P、R2 Port-X)

K 號:K201800 · 2020-12-28

決定日期2020-12-28
產品代碼EHD
諮詢委員會DE
決定相當於

器材摘要

Portable Dental X-ray (NR-F350, CS 2400P, CS 2300P, R2 Port-X) is the device name listed in this FDA 510(k) record. The listed applicant is Nanoray Co., Ltd.. It received FDA 510(k) clearance on 2020-12-28 under 510(k) number K201800. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Portable Dental X-ray (NR-F350, CS 2400P, CS 2300P, R2 Port-X)?

Portable Dental X-ray (NR-F350, CS 2400P, CS 2300P, R2 Port-X) is a medical device that received FDA 510(k) clearance on 2020-12-28. The listed applicant is Nanoray Co., Ltd.. The 510(k) number is K201800.

When did Portable Dental X-ray (NR-F350, CS 2400P, CS 2300P, R2 Port-X) receive FDA 510(k) clearance?

Portable Dental X-ray (NR-F350, CS 2400P, CS 2300P, R2 Port-X) received FDA 510(k) clearance on 2020-12-28, under 510(k) number K201800.

Who is the listed applicant for Portable Dental X-ray (NR-F350, CS 2400P, CS 2300P, R2 Port-X)?

The FDA 510(k) record lists Nanoray Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Portable Dental X-ray (NR-F350, CS 2400P, CS 2300P, R2 Port-X)?

The FDA product code for Portable Dental X-ray (NR-F350, CS 2400P, CS 2300P, R2 Port-X) is EHD.

相關臨床試驗

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相關器械(代碼:EHD)

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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