FDA 510(k)

ParaMotion

K-Number: K203761 · 2022-01-21

Decision Date2022-01-21

Product CodeIPL

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

ParaMotion is the device name listed in this FDA 510(k) record. The listed applicant is Powerbasetec GmbH. It received FDA 510(k) clearance on 2022-01-21 under 510(k) 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. The listed applicant is Powerbasetec GmbH. The 510(k) number is K203761.

When did ParaMotion receive FDA 510(k) clearance?

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

Who is the listed applicant for ParaMotion?

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

What is the FDA product code for ParaMotion?

The FDA product code for ParaMotion is IPL.

Related Devices (Code: IPL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243783Walking rehabilitation training electric wheelchair (ZW518)Shenzhen Zuowei Technology Co., Ltd.K202728Action Trackchair HawkAction Manufacturing, Inc.K191334Tek RMD (TEK ROBOTIC MOBILIZATION DEVICE) TEKRMD02, TEKRMD03, TEKRMD04, TEKRMD04, TEKRMD05, TEKRMD06, TEKRMD07, TEKRMD08Matia Robotics (Us), Inc.K190682Explorer MiniPermobil AB K191874F5 Corpus VSPermobil AB K182257UPnRIDEUpnride Robotics , Ltd.

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.