FDA 510(k)

KLICK（變種：POWER、RACE、MONSTER）

K 號：K222502 · 2022-12-16

決定日期2022-12-16

產品代碼ITI

諮詢委員會PM

決定相當於

器材摘要

KLICK (VARIANTS: POWER, RACE, MONSTER) is the device name listed in this FDA 510(k) record. The listed applicant is Klaxon Mobility GmbH. It received FDA 510(k) clearance on 2022-12-16 under 510(k) number K222502. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the KLICK (VARIANTS: POWER, RACE, MONSTER)?

KLICK (VARIANTS: POWER, RACE, MONSTER) is a medical device that received FDA 510(k) clearance on 2022-12-16. The listed applicant is Klaxon Mobility GmbH. The 510(k) number is K222502.

When did KLICK (VARIANTS: POWER, RACE, MONSTER) receive FDA 510(k) clearance?

KLICK (VARIANTS: POWER, RACE, MONSTER) received FDA 510(k) clearance on 2022-12-16, under 510(k) number K222502.

Who is the listed applicant for KLICK (VARIANTS: POWER, RACE, MONSTER)?

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

What is the FDA product code for KLICK (VARIANTS: POWER, RACE, MONSTER)?

The FDA product code for KLICK (VARIANTS: POWER, RACE, MONSTER) is ITI.

其他以 Klaxon Mobility GmbH 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。

K250748KLAXON (TWIST)；KLAXON (TWIST R)K240267Klaxon（扭動）；Klaxon（扭動 R）

相關器械（代碼：ITI）

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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