FDA 510(k)

KLICK (VARIANTS: POWER, RACE, MONSTER)

K-Number: K222502 · 2022-12-16

Decision Date2022-12-16

Product CodeITI

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by Klaxon Mobility GmbH. The 510(k) number is K222502.

When was KLICK (VARIANTS: POWER, RACE, MONSTER) approved by the FDA?

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

What company makes KLICK (VARIANTS: POWER, RACE, MONSTER)?

KLICK (VARIANTS: POWER, RACE, MONSTER) is manufactured by Klaxon Mobility GmbH.

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

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

Other Devices by Klaxon Mobility GmbH

K240267Klaxon (Twist); Klaxon (Twist R)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.