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Non-Powered Traction Apparatus Suppliers

 EMAIL INQUIRY to  141 to 142 of 142 suppliers  Page: << Previous 20 Results 1 2 3 4 5 6 7 [8]
A.M.G. Medical, Inc. | Address: 8505 Dalton Rd., Montreal, Quebec H4T-IV5, Canada Canada
www.amgmedical.com | Send Inquiry | Phone: (514)-737-5251, 888-396-1213
FDA Registration: 8022077  Annual Revenues: USD 10-25 Million  Employee Count: ~90
Products: Adhesive Strips & Patches, Skin Closure Adhesive Strips (FDA Code: FPX), Self Adhesive Strips (FDA Code: FPX), Alcohol Swabstick, Microfoam Adhesive Strip, Alcohol Swabs, ...
A.M.G. Medical, Inc. is a manufacturer and wholesale distributor of medical professional and home healthcare products. We are an ISO 9001 certified company, and licensed by Health Canada as well as re more...
 
Instituto De Ortopedia E Fisioterapia Sao Paulo Ltda | Address: Rua Antonio Victor Maximiano 107, Parque Industrial Ii, Santa Tereza Do Oeste 85825000, Brazil
Phone: +55-(45)-400-97044
Products: Examination and Treatment Chair (FDA Code: FRK), Exercise Component (FDA Code: IOD), Exercise Parallel Bars (FDA Code: IOE), Force-Measuring Platform (FDA Code: KHX), Manual Therapeutic Massager (FDA Code: LYG), Mechanical Table (FDA Code: INW), ...
Instituto De Ortopedia E Fisioterapia Sao Paulo Ltda deals with medical furnitures and accessories. Our products include examinations and treatment chairs, exercise components, exercise parallel bars more...
 EMAIL INQUIRY to  141 to 142 of 142 Non-Powered Traction Apparatus suppliers  Page: << Previous 20 Results 1 2 3 4 5 6 7 [8]
FDA Code / Regulation: HST / 888.5850

A nonpowered orthopedic traction apparatus is a device that consists of a rigid frame with nonpowered traction accessories, such as cords, pulleys, or weights, and that is intended to apply a therapeutic pulling force to the skeletal system.

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 888.9. 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.

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