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FDA 510(k)

ParaMotion

K-Number: K203761 · 2022-01-21

ApplicantPowerbasetec GmbH
Decision Date2022-01-21
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ParaMotion is a medical device manufactured by Powerbasetec GmbH. It received FDA 510(k) clearance on 2022-01-21 under approval number K203761. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ParaMotion?

ParaMotion is a medical device that received FDA 510(k) clearance on 2022-01-21. It is manufactured by Powerbasetec GmbH. The 510(k) number is K203761.

When was ParaMotion approved by the FDA?

ParaMotion received FDA 510(k) clearance on 2022-01-21, under approval number K203761.

What company makes ParaMotion?

ParaMotion is manufactured by Powerbasetec GmbH.

What is the FDA product code for ParaMotion?

The FDA product code for ParaMotion is IPL.

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Official Source

View on FDA Database →

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

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