Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Skin Pressure Protector Regulations

U.S. FDA Medical Device Skin Pressure Protector Requirements


FDA Medical Device Definition: A skin pressure protector is a device intended for medical purposes that is used to reduce pressure on the skin over a bony prominence to reduce the likelihood of the patient's developing decubitus ulcers (bedsores).

Registrar Corp assists Skin Pressure Protector companies with:

  • FDA Skin Pressure Protector Establishment Registration
  • FDA Skin Pressure Protector Listing
  • FDA Skin Pressure Protector Label Requirements and Exceptions
  • FDA Skin Pressure Protector Import Information
  • FDA Skin Pressure Protector Detentions (Skin Pressure Protector Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Skin Pressure Protector Manufacturers (Skin Pressure Protector Suppliers)
       - Skin Pressure Protector Distributors
       - Skin Pressure Protector Processors
       - Skin Pressure Protector Repackers
       - Skin Pressure Protector Relabelers
       - Skin Pressure Protector Exporters
       - Skin Pressure Protector Importers
For more information about Skin Pressure Protector Medical Devices, simply click below:






 
U.S. FDA Regulations:

U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.


Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2016 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco