← Product Code [IPL](/productcode/IPL) · K994083 # STANNAH POWER CHAIR, MODEL 201 (K994083) _Stannah Power Chairs , Ltd. · IPL · Apr 4, 2001 · Physical Medicine · SESE_ **Canonical URL:** https://fda.innolitics.com/device/K994083 ## Device Facts - **Applicant:** Stannah Power Chairs , Ltd. - **Product Code:** [IPL](/productcode/IPL.md) - **Decision Date:** Apr 4, 2001 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 890.3900 - **Device Class:** Class 2 - **Review Panel:** Physical Medicine - **Attributes:** Therapeutic ## Indications for Use The Stannah power Chair is intended as a device to provide personal transport for a person with walking difficulties. It is specifically designed to for indoor use in a domestic type environment. ## Device Story Stannah Power Chair Model 201 is a battery-powered, mid-wheel drive wheelchair designed for indoor domestic use. The device consists of a high-quality office chair mounted on a base assembly containing two drive motors, gearboxes, drive wheels, five castor wheels, and batteries. A proprietary controller unit with a joystick is attached to the seat for user-operated motion control. A gas strut allows for manual or optional powered height adjustment of the chair; powered adjustment is inhibited while the chair is in motion. The device is operated by the user to provide mobility. It provides personal transport for individuals with walking difficulties, enhancing maneuverability in domestic settings. ## Clinical Evidence Bench testing only. The device was tested for compliance with BS/ISO Powered Wheelchair Standard ISO 7176 (parts 1-16) and ISO EMC Draft Standard 7176-14. The device met all required performance criteria. ## Technological Characteristics Materials: Folded sheet steel base. Drive: Twin motor/gearbox, mid-wheel drive. Power: Battery-operated. Features: Gas strut for height adjustment, joystick controller. Standards: ISO 7176 parts 1-16, ISO 7176-14 (EMC). ## Regulatory Identification A standup wheelchair is a device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. The device incorporates an external manually controlled mechanical system that is intended to raise a paraplegic to an upright position by means of an elevating seat. ## Predicate Devices - Pride Health Care "Jazzy" Powered Wheelchair ([K945936](/device/K945936.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}------------------------------------------------ K 994083 10F > # APR - 4 2001 ## 510(k) SUMMARY # Stannah Power Chair Ltd. Model 201 Power Chair # Submitters Name, Address, Telephone Number, Contact Person and Date Prepared. Stannah Power Chairs Ltd. Watt Close East Portway Ind. Estate Andover Hampshire SP10 3SD England Contact Person: Charles Edgell Director Stannah Power Chairs Ltd December 1999 Date Prepared: # Name of Device and Name / Address of Sponsor Stannah Power Chair Model 201 Stannah Power Chairs Ltd. Watt Close East Portway Ind. Estate Andover Hampshire SP10 3SD England Common or Usual Name Powered Wheelchair ### Classification Name Wheelchair, Powered #### Predicative Devices Pride Health Care "Jazzy" Powered Wheelchair (510(k) # K 945936 date 05/28/94) {1}------------------------------------------------ ### Intended Use The Stannah power Chair is intended as a device to provide personal transport for a person with walking difficulties. It is specifically designed to for indoor use in a domestic type environment. ### Technological Characteristics and Substantial Equivalence ### Device Description: The Power Chair is a powered wheelchair based around a high quality office chair. Attached to the chair is a proprietary controller unit, which can be mounted on either side of the seat. The motion is operated by the user hand via a joystick. The attachment method allows the controller to be positioned further forward or backwards relative to the chair for comfort and convenience of the user. The chair is attached to a base assembly containing the drive motors, drive wheels, castor wheels and batteries, by a Gas Strut (anti-rotate) which enables the chair to be raised or lowered within set limits. Operation may be either manual, using a hand lever, or with a powered version option, via a separate control on the controller unit. The powered height adjustment can not be made while the power chair is driving in any direction. The Base is a profiled and of folded sheet steel fabrication, to which the two drive motor/gearboxes, two drive wheels, five castor wheels and a footrest assembly are mounted directly. #### Substantial Equivalence The Stannah Power Chair Model 201 is substantially equivalent to other devices of comparable type that are currently being legally marketed within the United States of America. The comparable device quoted and compared is the Pride Health Care "Jazzy" powered wheel chair, (510(k) # K 945936 date 05/28/94). Each of the products are battery powered, twin motor gearbox driven, mid wheel drive powered wheelchairs with the same intended function and use, which is to provide mobility to persons with walking difficulties, that have the capability of operating a powered wheelchair. They also offer excellent maneuverability due to their drive geometry. They are constructed of the same basic materials and have the same basic operational principles. ### Performance Data As required by the FDA's July 26th, 1995, draft publication entitled "Guidance Document for the Preparation of Pre-Market Notification [510(k)] Applications for Mechanical and Powered Wheelchairs, and Motorized Three Wheeled Vehicles". The Stannah Power Chair conforms to appropriate sections of BS/ISO Powered Wheelchair Standard #ISO 7176 parts 1-16. The Power Chair was also tested in accordance with the ISO EMC Draft Standard 7176-14, (titled "Draft ISO EMC Group Proposal: Electromagnetic Compatibility Addition" dated April 3rd, 1995) for Powered Wheelchairs and Scooters. In all instances, the Stannah Power Chair Model 201 met the required performance criteria and functioned as intended. K 99 4083 2002 {2}------------------------------------------------ Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized image of three human profiles facing to the right, stacked on top of each other. #### Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 APR - 4 2001 Mr. Charles Edgell Commercial Director Stannah Power Chairs LTD. Watt Close East Portway Ind. Estate Andover, Hampshire SP10 3SD England Re: K994083 Trade Name: Stannah Power Chair, Model 201 Regulatory Class: II Product Code: IPL Dated: February 8, 2001 Received: February 8, 2001 ### Dear Mr. Edgell: We have reviewed your Section 510(k) notification of intent to market the device referenced we have teviewed your bocally in the device is substantially equivalent (for the indications for use above and we nave acteringled an marketed in interstate commerce prior to May 28, 1976, the stated in the encrease) to device mansents, or to devices that have been reclassified in enacificin dato of the Modical Dottee Federal Food, Drug, and Cosmetic Act (Act). You may, accordance with the provisions of the general controls provisions of the Act. The general therefore, mainer the do reasjeve equirements for annual registration, listing of devices, controls provisions or use ice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations (1 tenance I reproval), it they over in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirement, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to mopolishing the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations. This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed nredicate device results in a classification for your device and thus, permits your device to proceed to the market. {3}------------------------------------------------ ### Page 2 - Mr. Charles Edgell If you desire specific advice for your device on our labeling regulation (21 CFF Part 801 and IT you desire specific active for your astic devices), please contact the Office of Compliance at additionally 607.10 for in This daglestions on the promotion and advertising of your device, (201) 594-4039. Additionally, for questions of (301) 594-4639. Also, please note the regulation prease connact the Office or Compilance at (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small information on your responsibilities under the Act 2011 442 (607 as stifs mornation on your responsibilities and its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address "http://www.fda.gov/cdrh/dsmamain.html". Sincerely yours, Mark N. Melkerson 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 of 1 510 (K) Number (If known): K994083 Device Name: Stannah Power Chair Model 201 Indications for Use: The Stannah Power Chair is intended as a device to provide personal The Stannan Fower Chair Is allement of the specifically transport for a for a for a domestic type environment. (Please do not write below this line - continue on another page if needed) Concurrence of CDRH, office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109) Over - the Counter - Use (Optional Format 1-2-96) L. Mark M. Milkman or (Division Sign-Off) (Division of General, Restorative and Neurological Devices 510(k) Number K994083 --- **Source:** [https://fda.innolitics.com/device/K994083](https://fda.innolitics.com/device/K994083) **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