Wheelchair Crutch and Cane Holder Suppliers
FDA Registration: 3007160937
Products: Medical Chair and Table (FDA Code: KMN), Crutch and Walker Cane Tips (FDA Code: INP), Mechanical Walker (FDA Code: ITJ), Wheelchair Crutch and Cane Holder (FDA Code: IMZ), ...
Foshan Nanhai Yingyou Metal Manufactory specializes in crutch and walker cane tips, and mechanical walkers. We also provide medical chair and table, and wheelchair crutch & cane holders. more...
Phone: +086-(757)-85502505
FDA Registration: 3007120364
Products: Adjustable Hospital AC-Powered Beds (FDA Code: FNL), Manual Beds (FDA Code: FNJ), Disabled/Handicapped Manual Wheelchair (FDA Code: IOR), Mechanical Wheelchair (FDA Code: IOR), Mechanical Adjustable Chair (FDA Code: INN), Mechanical Walker (FDA Code: ITJ), ...
Foshan City Nanhai Kaiyang Medical Equipment Co., Ltd deals with disabled/handicapped manual wheelchairs, mechanical adjustable chairs, mechanical walkers and mechanical wheelchairs. more...
www.parsonsadl.com | Send Inquiry | Phone: +1-(905)-936-3580
FDA Registration: 3003637065 Year Established: 1982 Annual Revenues: USD 1-5 Million Employee Count: ~20 Quality: ISO, CE Certified
Products: Arm Slings (FDA Code: ILI), Digital Wristwatch Style Blood Pressure Monitor, Bath Chair, Bedpan (FDA Code: FOB), Crutch (FDA Code: IPR), Disabled Grooming Adaptor (FDA Code: ILW), ...
Parsons A.D.L. Inc. offers a line of home health care products that assist persons with disabilities with activities of daily living. We provide a variety of bath chairs of various heights, bath board more...
A wheelchair accessory is a device intended for medical purposes that is sold separately from a wheelchair and is intended to meet the specific needs of a patient who uses a wheelchair. Examples of wheelchair accessories include but are not limited to the following: armboard, lapboard, pusher cuff, crutch and cane holder, overhead suspension sling, head and trunk support, and blanket and leg rest strap.
Classification. Class I (general controls). If the device is not intended for use as a protective restraint as defined in 880.6760 of this chapter, it is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 890.9. The device is also exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180, regarding general requirements concerning records, and 820.198, regarding complaint files.
