FDA 510(k)

Vave個人超音波系統

K 號：K191541 · 2019-07-10

決定日期2019-07-10

產品代碼IYO

諮詢委員會RA

決定相當於

器材摘要

Vave Personal Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Vave Health, Inc.. It received FDA 510(k) clearance on 2019-07-10 under 510(k) number K191541. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vave Personal Ultrasound System?

Vave Personal Ultrasound System is a medical device that received FDA 510(k) clearance on 2019-07-10. The listed applicant is Vave Health, Inc.. The 510(k) number is K191541.

When did Vave Personal Ultrasound System receive FDA 510(k) clearance?

Vave Personal Ultrasound System received FDA 510(k) clearance on 2019-07-10, under 510(k) number K191541.

Who is the listed applicant for Vave Personal Ultrasound System?

The FDA 510(k) record lists Vave Health, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vave Personal Ultrasound System?

The FDA product code for Vave Personal Ultrasound System is IYO.

其他以 Vave Health, Inc. 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。

K241051Vave無線超音波系統

相關器械（代碼：IYO）

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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官方來源

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