← Product Code [INI](/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI) · K033116 # OPTI-RIDER DELUXE (K033116) _Hansung Econet Co., Ltd. · INI · Apr 12, 2004 · Physical Medicine · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI/K033116 ## Device Facts - **Applicant:** Hansung Econet Co., Ltd. - **Product Code:** [INI](/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI.md) - **Decision Date:** Apr 12, 2004 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 890.3800 - **Device Class:** Class 2 - **Review Panel:** Physical Medicine ## Indications for Use The Opti-Rider Deluxe is a motorized, battery-operated, four-wheel scooter used for transportation by disabled persons. ## Device Story Opti-Rider Deluxe is a battery-operated, four-wheeled motorized scooter for transportation of disabled persons. Device comprises a motorized chassis, drive unit, steering column, braking system, and electronics control module. User sits on a chassis-mounted seat and operates the vehicle via hand controls and a console located on the steering column. Console manages speed, direction, horn, headlight, and directional signals. Electric braking system defaults to 'on' and disengages upon throttle activation. Device includes an on-board battery charger. Used by the patient for mobility; provides independent transportation. ## Clinical Evidence Bench testing only. Device demonstrated conformance with FDA's 'Guidance Document for the Preparation of Premarket Notification [510(k)] Applications for Mechanical and Powered Wheelchairs, and Motorized Three-Wheeled Vehicles' and ANSI/RESNA W/C Vol. 2 - 1998, Section 21. ## Technological Characteristics Motorized four-wheeled chassis; electric braking system (default 'on'); battery-operated with on-board charger; steering column-mounted console for speed/direction control. Conforms to ANSI/RESNA W/C Vol. 2 - 1998, Section 21. ## 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 - C.T.M. Mobility Scooter HS-686 ([K983662](/device/K983662.md)) - Mega 4 Scooter ([K982144](/device/K982144.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}------------------------------------------------ Image /page/0/Picture/2 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle or bird symbol, with three curved lines representing the wings and body. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged in a circular fashion around the bird symbol. The logo is black and white. MAY 4 - 2004 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Hansung Econet Co. Ltd. C/o Mr. Sanghun Kim Econet USA, Inc. 11 Mill Creek Irvine, California 92612 Re: K033116 Trade/Device Name: Opti-Rider Deluxe Regulation Number: 21 CFR 890.3800 Regulation Name: Motorized three-wheeled vehicle Regulatory Class: II Product Code: INI Dated: February 25, 2004 Received: February 25, 2004 Dear Mr. Kim: This letter corrects our substantially equivalent letter of March 12, 2004 regarding the device named above. The letter was incorrectly addressed to Hansug Econet Co. Ltd. Hansung Econet Co. Ltd is the correct addressee. 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 (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 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. {1}------------------------------------------------ Page 2 - Mr. Sanghun Kim This letter will allow you to continue 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 Mark N. Milburn 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 {2}------------------------------------------------ u.0(4 r.1/2 K033116/A00 V # Indications for Use 510(k) Number (if known) : K033116 Device Name : Propristary Name : Opti-Rider Deluxe Common/Usual Name : Scooter Classilication Name : Motorized three-whecled vehicle Indications For Use: : The Coti-Rider Deluxe is a motorized, battery-operated, fourwheel scooter used for transportation by disabled persons. The p:inciples of operation of the proposed Opti-Rider Deluxe are idiantical to those of the predicate C.T.M. Mobility Scooter HS-686 scooter and other motorized vehicles legally marketed in the U.S. for use by disabled persons for transportation purposes. The Opti-Rider Deluxe, and other motorized fourwheeled vehicles, consists of a motorized chassis with a battery, drive unit, steering column, and electronics module. The user sits in a seat mounted on the chassis and operates the scooter via handpieces mounted on the steering column that also contains the console for control of the speed, emergency brake, and other features. March 16, 2004 Hong-Seok Kim / President Hong-Seok Kim / President Prescription Use AND/OR (Part 21 CFR 801 Subpar k) Numb Over-The-Counter Use (21 CFR 807 Subpart C) BELOW THIS LINE-CONTINUE ON (PI FASE DO NOT ANOTHER PAGE IF Concurrence of CDRH, Office of Device Evaluation (ODE) Page 1 of 1 KC^{29} {3}------------------------------------------------ K033116 APR 1 2 2004 # 510(k) Summary for OPTI-RIDER DELUXE #### 1. SPONSOR HANSUNG ECONFT Co., Ltd. #168, Wonnam-ri Umbong-myon Asan Chungnam 336-864 Korea Contact Person: Hong-Seok Kim, President Telephone: 82-41 541 5733 Date Prepared: September 29, 2003 # 2. DEVICE NAME Proprietary Name: Opti-Rider Deluxe Common/Usual Name: Scootcr Classification Name: Motorized three-wheeled vchicle # 3. PREDICATE DEVICES - C.T.M. Mobility Scooter HS-686 (K983662) . - Mega 4 Scooter (K982144) . #### 4. DEVICE DESCRIPTION The proposed Opti-Rider Deluxe consists of a motorized, four-wheeled chassis with batteries, drive unit, steering column, braking system, and electronics module for operational control of the vehicle. The user sits in a seat mounted on the chassis and operates the scooter via hand controls and a console mounted on the steering column. # 5. INTENDED USE The Opti-Rider Deluxe is a motorized, battery-operated, four-wheel scooter used for transportation by disabled persons. {4}------------------------------------------------ #### 6. TECHNOLOGICAL CHARACTERISTICS AND SUBSTANTIAL EQUIVALENCE The proposed and predicate devices consist of a motorized chassis with four wheels, drive unit, steering column, and electronics module. The user sits in a seat mounted on the chassis and operates the scooter via hand controls mounted on the steering column. The steering column for the proposed and prodicate devices also houses a console and controls for functions including specd, direction of travel, and features such as the horn, headlight, and directional signals. There are minor differences in the placement of these controls on the stecring column, and the organization of the console, between the proposed and predicate devices. The proposed Opti-Rider Deluxe and the predicate C.T.M. Mobility and Mega 4 Scooters have an clectric braking system. The default status of the brakes is "on," and is disengaged only when the operator moves the throttle to place the scooter in motion. Both the proposed and predicate devices are battery-operated and have on-board battery chargers. Performance characteristics such as maximum forward and reverse speed, turning radius, maximum safe incline, ctc., are similar between the proposed and predicate devices. # 7. PERFORMANCE TESTING The Opti-Rider Deluxe was tested to demonstrate conformance with the requirements of FDA's "Guidance Document for the Preparation of Premarket Notification [510(k)] Applications for Mechanical and Powered Wheelchairs, and Motorized Three-Wheeled Vchicles," issued July 6, 1995, and reformatted December 18, 1997. The Opti-Rider Deluxe is in compliance with the applicable requirements of ANSI/RESNA W/C Vol. 2 - 1998, Section 21. --- **Source:** [https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI/K033116](https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI/K033116) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. 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