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FDA 510(k)

Action Trackchair Hawk

K-Number: K202728 · 2022-02-10

ApplicantAction Manufacturing, Inc.
Decision Date2022-02-10
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Action Trackchair Hawk is the device name listed in this FDA 510(k) record. The listed applicant is Action Manufacturing, Inc.. It received FDA 510(k) clearance on 2022-02-10 under 510(k) number K202728. 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 Action Trackchair Hawk?

Action Trackchair Hawk is a medical device that received FDA 510(k) clearance on 2022-02-10. The listed applicant is Action Manufacturing, Inc.. The 510(k) number is K202728.

When did Action Trackchair Hawk receive FDA 510(k) clearance?

Action Trackchair Hawk received FDA 510(k) clearance on 2022-02-10, under 510(k) number K202728.

Who is the listed applicant for Action Trackchair Hawk?

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

What is the FDA product code for Action Trackchair Hawk?

The FDA product code for Action Trackchair Hawk is IPL.

Other records listing Action Manufacturing, Inc. as applicant

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.

K181908Action TrackchairK163451Action Trackstander models TR1816, TR1820, TR2016, and TR2020

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.K203761ParaMotionPowerbasetec GmbHK191334Tek RMD (TEK ROBOTIC MOBILIZATION DEVICE) TEKRMD02, TEKRMD03, TEKRMD04, TEKRMD04, TEKRMD05, TEKRMD06, TEKRMD07, TEKRMD08Matia Robotics (Us), Inc.K190682Explorer MiniPermobil ABK191874F5 Corpus VSPermobil ABK182257UPnRIDEUpnride Robotics , Ltd.

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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