Homemaking Utensil Suppliers
Phone: +86-(516)-4829001
FDA Registration: 3006984916
Products: Cardiopulmonary Resuscitation Emergency Cart (FDA Code: BZN), Handicapped Cane (FDA Code: IPS), Crutch (FDA Code: IPR), Crutch and Walker Cane Tips (FDA Code: INP), Disabled/Handicapped Hygiene Adaptor (FDA Code: ILS), Mechanical Table (FDA Code: INW), ...
Fort Metal Plastic Co., Ltd. offers cardiopulmonary resuscitation emergency cart, crutch and walker cane tips, disabled and handicapped hygiene adapter & handicapped cane. We also supply mechanical wa 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...
Phone: (514)-739-1310
Annual Revenues: < USD 1 Million
Products: Bed Transfer Aids, Transfer Aid for Disabled/Handicapped (FDA Code: IKX), Transfer Aid (FDA Code: IKX), Exercise Component (FDA Code: IOD), Disabled Grooming Adaptor (FDA Code: ILW), Homemaking Utensil (FDA Code: IKW), ...
Wolspal Inc. supplies surgical appliances. We specialize in the production of orthopedic appliances. more...
A daily activity assist device is a modified adaptor or utensil (e.g., a dressing, grooming, recreational activity, transfer, eating, or homemaking aid) that is intended for medical purposes to assist a patient to perform a specific function.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 890.9. If the device is not labeled or otherwise represented as sterile, 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.
