← Product Code [INI](/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI) · K033032 # WU'S 3-WHEELED NEO SCOOTER, MODEL WT-M3JR (K033032) _Wu'S Tech Co., Ltd. · INI · Nov 10, 2003 · Physical Medicine · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI/K033032 ## Device Facts - **Applicant:** Wu'S Tech Co., Ltd. - **Product Code:** [INI](/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI.md) - **Decision Date:** Nov 10, 2003 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 890.3800 - **Device Class:** Class 2 - **Review Panel:** Physical Medicine - **Attributes:** Therapeutic ## Indications for Use The device is intended for medical purposes to provide mobility to persons restricted to a seated position. ## Device Story Battery-operated 3-wheeled electric scooter; provides mobility for individuals restricted to seated position. Rider operates via hand controls on steering column. Features seat, armrests, front basket; disassembles for transport. Includes onboard battery charger. Used in indoor/outdoor environments. Output is physical mobility for patient. Safety verified via EMC testing per ANSI/RESNA WC/Vol.2-1998 and related IEC/EN standards. ## Clinical Evidence Bench testing only. Compliance with EMC and safety standards (ANSI/RESNA WC/Vol.2-1998, CISPR 11, EN61000-3-2, IEC61000-3-3) for electrically powered scooters. ## Technological Characteristics Battery-operated electric scooter; 3-wheeled configuration; hand-controlled steering column; modular design for disassembly. Electronic systems (controller, batteries, charger) are UL certified. Tested to ANSI/RESNA WC/Vol.2-1998, CISPR 11: 1990, EN61000-3-2: 1995, and IEC61000-3-3: 1995 standards. ## Regulatory Identification A motorized three-wheeled vehicle is a gasoline-fueled or battery-powered device intended for medical purposes that is used for outside transportation by disabled persons. ## Predicate Devices - WU'S 3-WHEELED NEO SCOOTER WT-M3 ([K014119](/device/K014119.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ K033032 1/ August 23, 2003 NOV 1 0 2003 ## NO. 225, YUAN-PIER S TEL: 886-5-5382105 Homepage: www.wustech.com.tw tis@ms45.hinet.net ## 510(k) SUMMARY " ર્દ Submitter's Name: WU'S TECH CO., LTD. NO. 225, YUAN-PIER ST., HSIN CHU CITY, CHINA (TAIWAN) Tel: 88 Date summary prepared: Device Name: | Proprietary Name: | WU'S 3-Wheeled Scooter, WT-M3Jr | |-----------------------|---------------------------------------------------------| | Common or Usual Name: | Electrical Scooter | | Classification Name: | Motor Three-Wheeled Vehicle, Class II, 21 CER 890 3800 | Indications for Use: The device is intended for medical purposes to provide mobility to persons restricted to a seated position. Description of the device: The WU'S 3-WHEELED SCOOTER WT-M3Jr is an indoor / outdoor electric scooter that is battery operated. It has a base with four-wheeled with a seat, armrests, and a front basket. The movement of the scooter is controlled by the rider who uses hand controls located at the top of the steering column. The device can be disassembled for transport and is provided with an onboard battery charger. Performance Testing: EMC Report ANSI / RESNA WC/Vol.2-1998, CISPR 11: 1990, EN61000-3-2: 1995, IEC61000-3-3: 1995 (Electrically powered wheelchairs, scooters, and their chargers - requirements and test methods) Legally marketed device for substantial equivalence comparison: WU'S 3-WHEELED NEO SCOOTER WT-M3 (K014119) {1}------------------------------------------------ K033032 2/2 NO. 225, YUAN-PIER ST., HSIN CHU CITY, CHIN FAX: 886-5-53821 TEL: 886-5-5382105 Homepage: www.wustech.com.tw Email: wustis@ms45.hinet.net Summary for substantial equivalence comparison: The electronic systems between two devices are the same and all passed by the UL certificated, for instance the electronic controller, batteries and recharge. Thus the same safety level for the two devices is assured. The major differences existing of the two 3-wheelled scooters are the different controller, and the new device, WT-M3Jr, is more agile and easy to storage or transportation and the predicate device, WT-M3, is for general use. Besides the overall dimension, the size of tires, and the weight are differences between the two devices. The overall appearance differences are not safety aspect. So the new device is substantially equivalent to the predicate devices in this aspect. {2}------------------------------------------------ Image /page/2/Picture/1 description: The image is a black and white circular logo for the U.S. Department of Health & Human Services. The logo features a stylized image of an eagle with three lines representing its wings and head. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged around the top half of the circle. NOV 1 0 2003 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 WU'S Tech. Co., LTD C/o Dr. Ke-Min Jen ROC Chinese-European Industrial Research Society No. 58. Fu-Chiun St. Hsin-Chu City, China (Taiwan) 300 Re: K033032 Trade/Device Name: WU'S 3-Wheeled NEO Scooter, WT-M3Jr Regulation Number: 21 CFR 890.3800 Regulation Name: Motorized three-wheeled vehicle Regulatory Class: II Product Code: INI Dated: October 16, 2003 Received: October 23, 2003 Dear Dr. Jen: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (PMA). it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. {3}------------------------------------------------ Page 2 -- Dr. Ke-Min Jen This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus. permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (301) 594-4659. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html Sincerely yours, Miriam C. Provost for Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ Page 1 loof of 1 l 510 (K) NUMBER(IF KNOWN): TBA WIJ'S 3-WHEELED NEO SCOOTER, WT-M3Jr > DEVICE NAME: INDICATIONS FOR USE: The device is intended for medical purposes to provide mobility to persons restricted to a seated position. ( PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE Concurrence of CDRH, office of Device Evaluation (ODE ) Prescription Use _____________________________________________________________________________________________________________________________________________________________ OR Over-The-Counter-Use ( Per 21 CFR 801.109 ) ( Optional Format 1-2-96 ) Miriam C. Provost 510(k) Number K033032 ।र । --- **Source:** [https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI/K033032](https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI/K033032) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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