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FDA 510(k)

PENTAX醫療 ED-3490TK 電子十二指腸鏡

K 號:K192280 · 2019-10-21

決定日期2019-10-21
產品代碼FDT
諮詢委員會GU
決定相當於

器材摘要

PENTAX Medical ED-3490TK Video Duodenoscope is the device name listed in this FDA 510(k) record. The listed applicant is Pentax Medical. It received FDA 510(k) clearance on 2019-10-21 under 510(k) number K192280. The device is classified under product code FDT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the PENTAX Medical ED-3490TK Video Duodenoscope?

PENTAX Medical ED-3490TK Video Duodenoscope is a medical device that received FDA 510(k) clearance on 2019-10-21. The listed applicant is Pentax Medical. The 510(k) number is K192280.

When did PENTAX Medical ED-3490TK Video Duodenoscope receive FDA 510(k) clearance?

PENTAX Medical ED-3490TK Video Duodenoscope received FDA 510(k) clearance on 2019-10-21, under 510(k) number K192280.

Who is the listed applicant for PENTAX Medical ED-3490TK Video Duodenoscope?

The FDA 510(k) record lists Pentax Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PENTAX Medical ED-3490TK Video Duodenoscope?

The FDA product code for PENTAX Medical ED-3490TK Video Duodenoscope is FDT.

相關臨床試驗

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其他以 Pentax Medical 為申請人之記錄

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相關器械(代碼:FDT)

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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