FDA 510(k)

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K 號：K223244 · 2022-12-21

決定日期2022-12-21

產品代碼HRX

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決定相當於

器材摘要

Pristine Arthroscopic Visualization System is the device name listed in this FDA 510(k) record. The listed applicant is Pristine Surgical. It received FDA 510(k) clearance on 2022-12-21 under 510(k) number K223244. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Pristine Arthroscopic Visualization System?

Pristine Arthroscopic Visualization System is a medical device that received FDA 510(k) clearance on 2022-12-21. The listed applicant is Pristine Surgical. The 510(k) number is K223244.

When did Pristine Arthroscopic Visualization System receive FDA 510(k) clearance?

Pristine Arthroscopic Visualization System received FDA 510(k) clearance on 2022-12-21, under 510(k) number K223244.

Who is the listed applicant for Pristine Arthroscopic Visualization System?

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

What is the FDA product code for Pristine Arthroscopic Visualization System?

The FDA product code for Pristine Arthroscopic Visualization System is HRX.

其他以 Pristine Surgical 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。

K193161純淨範圍 K183165純淨範圍

相關器械（代碼：HRX）

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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