← Product Code [INI](/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI) · K051116 # MODEL TL-560 POWER SCOOTER (K051116) _Teh Lin Prosthetic & Orthopaedic, Inc. · INI · May 31, 2005 · Physical Medicine · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI/K051116 ## Device Facts - **Applicant:** Teh Lin Prosthetic & Orthopaedic, Inc. - **Product Code:** [INI](/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI.md) - **Decision Date:** May 31, 2005 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 890.3800 - **Device Class:** Class 2 - **Review Panel:** Physical Medicine ## Indications for Use The device is intended for medical purposes to provide mobility to persons restricted to a seated position. ## Device Story TEH LIN Power Scooter (TL-560) is a battery-operated, four-wheeled indoor/outdoor mobility device. Rider operates scooter via hand controls on steering column. Device features foldable frame, removable armrests, and onboard battery charger. Intended for individuals restricted to seated position to provide mobility. Healthcare provider role is limited; device is for patient use. Benefits include improved mobility and independence for users with restricted physical capacity. ## Clinical Evidence Bench testing only. Compliance with ANSI/RESNA WC/Vol.2-1998, CISPR 11: 1990, EN61000-3-2: 1995, and IEC61000-3-3: 1995 for electromagnetic compatibility and performance of powered scooters, controllers, and chargers. ## Technological Characteristics Four-wheeled battery-operated scooter. Features Penny & Giles EGIS control system. Materials include upholstery passed for resistance ignition per SGS testing. Dimensions, weight capacity, and cruising range vary from predicate. Connectivity: None. Energy source: Battery. ## 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 - TEH LIN POWER SCOOTER TL-821 ([K042011](/device/K042011.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}------------------------------------------------ ## KOSIII 6 ## TEH LIN PROSTHETIC & ORTHOPAEDIC INC. No. 7, Wu Chuan 7th Road, WuKu Industrial Park, MAY 3 1 2005 Taipei County, Taiwan R.O.C. Telephone: 886-2-22991901 Fax: 886-2-22991030 E-mail: tlco@ms2.hinet.net http://www.tehlin.com.tw #### 510(k) SUMMARY " દ દ ### Submitter's Name: TEH LIN Prosthetic & Orthopaedic Inc. No. 7, Wu Chuan 7th Road, WuKu Industrial Park, Taipei County, Taiwan R.O.C. April 25, 2005 Date summary prepared: Device Name: Proprietary Name: Common or Usual Name: Classification Name: TEH LIN Power Scooter, TL-560 Powered Scooter Powered Scooter, Class II, 21 CFR 890.3860 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 TEH LIN Powered Scooter, TL-560 is an indoor / outdoor Powered Scooter that It has a base with four-wheeled with a seat. is battery operated. The movement of the Scooter is controlled by the rider who uses hand controls located at the top of the The device can be disassembled for transport and is provided with steering column. 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 Scooters, controller, and their chargers requirements and test methods) Legally marketed device for substantial equivalence comparison: TEH LIN POWER SCOOTER TL-821 (K042011) {1}------------------------------------------------ # TEH LIN PROSTHETIC & OF No. 7, Wu Chuan 7th Road, WuKu Industrial Park, Taipei County, Taiwan R.O.C. Telephone: 886-2-22991901 Fax: 886-2-22991030 E-mail: tlco@ms2.hinet.net http://www.tehlin.com.tw Summary for substantial equivalence comparison: The intended use between the two devices is the same. The batteries used are the same brand that is certified by UL. The control systems for the two devices are same brand i.e., Penny & Giles EGIS type for the two devices. The recharge for the two devices are used the same resource, and the recharge is certified by UL. Besides, the foldable frame, the maximum speed, removable arm type, same warranty on component and frame, and back upholstery are the same material that also be passed the resistance ignition test by SGS. Thus the same safety level for the two devices is assured. The major differences existing of the two Power Scooters are the different overall dimension, tires, seat size, weight limit, weight capabilities, safe climbing angle, and cruising range between the two devices. Based on the above the information and the analysis, we know that the subject device and the predicate device have the same intended use, the same technological aspects and only minor differences exist. So the new device is substantially equivalent to the predicate devices in this aspect. {2}------------------------------------------------ DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH AND HUMAN SERVICES, USA" around the perimeter. Inside the circle is an abstract image of an eagle or bird-like figure with three stylized lines representing its wings or feathers. Public Health Service MAY 3 1 2005 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Teh Lin Prosthetic and Orthopaedic Incorporated C/o Dr. Ke-Min Jen Chinese-European Industrial Research Society No. 58 Fu-Chiun Street Hsin Chu City, China (Taiwan) 300 Re: K051116 Trade/Device Name: TEH LIN Power Scooter, TL-560 Regulation Number: 21 CFR 890.3800 Regulation Name: Motorized three-wheeled vehicle -Regulatory Class: II Product Code: INI Dated: April 25, 2005 Received: May 2, 2005 Dear Dr. Jen: We have reviewed your Section 510(k) premarket notification of intent to market the device we nave roviewed your been mind the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate for use bated in the May 28, 1976, the enactment date of the Medical Device Amendments, or to conimer of the have been reclassified in accordance with the provisions of the Federal Food, Drug, de nees that have been rout 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 r ou may , mere over in 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 r read o o a roude a determination that your device complies with other requirements of the Act that I Drederal 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 Of N Fart 677, huolity 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) I this letter will anow you to begin maniesing your and equivalence of your device to a legally premiter notification: "The 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 If you desire specific advice for your ac (240) 276-0120 . Also, please note the regulation entitled, colliation of Compulance in (21 the Part 807.97). You may obtain Misolanding by reference to premains. Fibilities under the Act from the Division of Small other general informational and Consumer Assistance at its toll-free number (800) 638-2041 or Manufacturers, Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely yours, Miriam C. Provost, Ph.D. Miriam C. Provost, Ph.D. Acting Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ ## Indications for Use 510 (K) Number ( If Known ): _________________________________________________________________________________________________________________________________________________ Device Name: TEH LIN Power Scooter, TL-560_ Indications for Use: The device is intended for medical purposes to provide mobility to persons restricted to a sitting position. Prescription Use _____________________________________________________________________________________________________________________________________________________________ AND/OR Over-The-Counter Use __ V (Part 21 CFR 801 Subpart D) (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Styet Rhodes Sign-Off (Division Division of General, Restorative, and Neurological Devices Page 1 _of _1 FI 510(k) Number_________________________________________________________________________________________________________________________________________________________________ --- **Source:** [https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI/K051116](https://fda.innolitics.com/submissions/PM/subpart-d%E2%80%94physical-medicine-prosthetic-devices/INI/K051116) **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. If you're preparing [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/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com