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FDA 510(k)

無壓力印象

K 號:K213175 · 2023-01-19

決定日期2023-01-19
產品代碼ELW
諮詢委員會DE
決定相當於

器材摘要

No Stress Impress is the device name listed in this FDA 510(k) record. The listed applicant is No Stress Impress, LLC. It received FDA 510(k) clearance on 2023-01-19 under 510(k) number K213175. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the No Stress Impress?

No Stress Impress is a medical device that received FDA 510(k) clearance on 2023-01-19. The listed applicant is No Stress Impress, LLC. The 510(k) number is K213175.

When did No Stress Impress receive FDA 510(k) clearance?

No Stress Impress received FDA 510(k) clearance on 2023-01-19, under 510(k) number K213175.

Who is the listed applicant for No Stress Impress?

The FDA 510(k) record lists No Stress Impress, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for No Stress Impress?

The FDA product code for No Stress Impress is ELW.

相關臨床試驗

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相關器械(代碼:ELW)

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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