RUIKE, MODEL 3431

K062645 · Shanghai Ruike Sports Goods Co., Ltd. · INI · Dec 19, 2006 · Physical Medicine

Device Facts

Record IDK062645
Device NameRUIKE, MODEL 3431
ApplicantShanghai Ruike Sports Goods Co., Ltd.
Product CodeINI · Physical Medicine
Decision DateDec 19, 2006
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 890.3800
Device ClassClass 2

Indications for Use

The Ruike 3431 scooter is motor driven, indoor and outdoor transportation vehicles with the intended use to provide mobility to disabled or elderly persons limited to a seated position.

Device Story

Ruike 3431 is a battery-operated, motorized three-wheeled scooter for indoor/outdoor transportation of disabled or elderly individuals. Device features a tiller handle and thumb-operated potentiometer throttle control to manage forward and reverse motion. It utilizes a sealed transaxle direct drive system and PG S-Drive 45A controller. The scooter is designed for seated operation; it provides mobility assistance to users, potentially improving independence. It is intended for use by the patient.

Clinical Evidence

No clinical data provided; bench testing only.

Technological Characteristics

Motorized three-wheeled vehicle; battery-operated (12V x 2); PG S-Drive 45A controller; sealed transaxle direct drive; steel frame construction; solid tires; thumb-operated potentiometer throttle; regenerative electromagnetic braking system.

Indications for Use

Indicated for disabled or elderly persons limited to a seated position requiring indoor/outdoor mobility assistance.

Regulatory Classification

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

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ DEC 1 9 2006 K062645 Page 1 of 4 # Shanghai Ruike Sports Goods CO., LTD. FAX: +86-21-66351873 No. 689, Xinhu Road, Shanghai, China TEL: +86-21-66350714 ## 510(k) Summary ### Device Trade name: Ruike 3431 scooter Common name: Electrical scooter Classification name: Motorized three-wheeled vehicle Medical specialty (Panel): Physical Medicine Device Regulation number: 890.3800 Product Code: 89INI Classification: Class II #### Predicate devices ## Bewell SC 20 (K043326)/Cycling and Health Tech Industry R&D Center/CHC Intend use of device Ruike 3431 scooter is intended for an indoor/outdoor scooter that provides transportation for disabled or elderly persons limited to a seated position. #### Device description: The Ruike 3431 scooter is an indoor/outdoor transportation vehicles which is battery operated. The movement of the scooter is controlled by a tiller handle and a thumb operated potentiometer throttle control lever to engage and disengage the scooter motion in both the forward and reverse directions. #### Substantial equivalence: The Ruike 3431 scooter is substantially equivalent to the Bewell SC 20 (K043326) manufactured by Cycling and Health Tech Industry R&D Center/CHC. There are minor differences in performance specifications of the scooters, these differences do not alter the intended function and use of the device, nor do they raise any new questions pertaining to safety or effectiveness. Therefore, Shanghai Ruike Sports Goods CO., LTD. believes that the Ruike 3431 scooter is substantially equivalent to legally marketed devices currently in commercial distribution. {1}------------------------------------------------ No. 689, Xinhu Road, Shanghai, China TEL: +86-21-66350714 FAX: +86-21-6635187 hanghai Ruike Sports Goods CO., LTD. | | Bewell SC 20(K043326) | Ruike 3431 | |---------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------| | Intended use | Both scooters are motor driven, indoor and outdoor transportation vehicles with the intended use to provide<br>mobility to disabled or elderly persons limited to a seated position. | | | Maximum loading | 130 kg (286 lbs) | 120 kg (265 lbs) | | Overall height | 1120 mm (44") | 825 mm (32.5") | | Overall length | 1300 mm (51.2") | 1030 mm (40.6") | | Overall width | 610 mm (24") | 510mm (20") | | Seat overall height | 370 mm (14.5") | 430 mm (16.9") | | Seat overall width | 450mm (17.7") | 500 mm (19.7") | | Seat overall depth | 450mm (17.7") | 400 mm (15.7") | | Seat overall weight | 7.5 kg (16.5 lbs) | 10 kg (22 lbs) | | Motor output | DC24V, 700W, 5000 RPM, 1Pc | 180 W x DC 24V, 1Pc | | Controller | Dynamic DS72K01 | PG S-Drive 45A | | Differential<br>mechanism | Differential rate: 20 : 1 | Differential rate: 17 : 1 | | Rear wheel drive | | Sealed transaxle direct drive | he substantial equivalence comparison of the Ruike 3431 and Bewell SC {2}------------------------------------------------ FAX: +86-21-663518 nghai Ruike Sports Goods CO., LT 689, Xinhu Road, Shanghai, China TEL: +86-21-66350714 x 80 mm(7.6"× 3.15") Solid tire x 2 80 mm(7.6"× 3.15") Solid tire x 2 ont/Rear: Yes, it's constructed by steel Ruike 34 ON on Automatic Type) off-be ead-Acid 12V×24AH×2 humb operated potentiometer throttle control ubstantial equivalence comparison of the Ruike 3431 and Bewell Foldable Yes Yes Yes No es, 4V 5AMP (Automatic Type) off-bo well SC 20(K04332 ont: Yes, it's constructed by steel 2V × 36AH × 2PCs 4" Pneumatic tire × 2 Pe 4" Pneumatic tire × 2 Po les ടുറു aluminum allo aluminum alle ead-Acid Rear : No les eight adjustab Backrest recline angle Recline angle peration moc Battery level ller foldabl ront whee Rear whee ontinuous ndicato Bumpers Headres rmres "harger Battery 20 and better like the comparison of substantial equivalence. K062645 Page 3 of 4 {3}------------------------------------------------ FAX: +86-21-663518 nghai Ruike Sports Goods CO., LT 689, Xinhu Road, Shanghai, China TEL: +86-21-6635071 ights and signal lights of the SC 20 and Ruike 3431 scooters have the same fur. tions, but only the Single mode, Variab Ruike 34 Rear: les m/hr (3.7 mph) , variab 05 m(41.3") at max sp ont: Yes(Optional), ntelligent regenerative electromagnetic br 000 mm (39.4" .5 km (9 mile kg (112 lbs 5 mm (1.8' 2 degree Yes Yes Yes ard: 2.58 m(101.6") at max spee ewell SC 20(K04331 ingle mode, Varial o 9 km/hr (5.6 mph), varia No to 35.2 km (22 mi ront: Yes, Rear: N kg (213 lbs 500 mm (59) 27 mm (5.0) re differen 2 degre r-charge distan lope grade abilit Braking distance Net weight with battery laximum spee urning radius faximum cur nti-tip wheel reak systen Varning ligh peed mode isassemble Tail lights Signal ligh uspensio Continuous 1eight Horn ibstantial equivalence comparison of the Ruike 3431 and Bewell K062645 Page 4 of 4 \$ 7\$ {4}------------------------------------------------ Image /page/4/Picture/13 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with its wings spread, and the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" are arranged in a circle around the eagle. The eagle is black, and the text is also black. The logo is simple and recognizable. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Shanghai Ruike Sports Goods Co., Ltd. % Ms. Junnata Chang 14F-2. No. 1. Lane 25 Banqiao, Taipei County, China (Taiwan) 220 DEC 1 9 2006 Re: K062645 Trade/Device Name: Ruike 3431 Regulation Number: 21 CFR 890.3800 Regulation Name: Motorized three wheeled vehicle Regulatory Class: Class II Product Code: INI Dated: December 12, 2006 Received: December 12, 2006 Dear Ms. Junnata Chang: 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. {5}------------------------------------------------ Page 2 -Ms. Junnata Chang 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 (240) 276-0120 . 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 (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely yours, F-n P Mark N. Mellekerson Mark N. Melkerson Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {6}------------------------------------------------ #### 3. Device descriptive information 3.1 Statement of indication for use ## Statement of Indications for Use 1062645 510(k) Number (if known): Device Name: Ruike 3431 Indications for Use: The Ruike 3431 scooter is motor driven, indoor and outdoor transportation vehicles with the intended use to provide mobility to disabled or elderly persons limited to a seated position. Over-The-Counter Use _ X Prescription Use (Part 21 CFR 807 Subpart C) (Part 21 CFR 801 Subpart D) AND/OR (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED) Concurrence of CDRIA Office of Device Evaluation (ODE) Page 1 of 1 **(Division Sign-Off)** (Division of General, Restorative and Neurological Devices 510(k) Number (Posted November 13, 2003)
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