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U.S. FDA Medical Device Electric Cystometric Table Requirements


FDA Medical Device Definition: A urological table and accessories is a device that consists of a table, stirrups, and belts used to support a patient in a suitable position for endoscopic procedures of the lower urinary tract. The table can be adjusted into position manually or electrically.

Registrar Corp assists Electric Cystometric Table companies with:

  • FDA Electric Cystometric Table Establishment Registration
  • FDA Electric Cystometric Table Listing
  • FDA Electric Cystometric Table Label Requirements and Exceptions
  • FDA Electric Cystometric Table Import Information
  • FDA Electric Cystometric Table Detentions (Electric Cystometric Table Entry Refusals)
  • General U.S. Food and Drug Administration Medical Device Guidelines for:
       - Electric Cystometric Table Manufacturers (Electric Cystometric Table Suppliers)
       - Electric Cystometric Table Distributors
       - Electric Cystometric Table Processors
       - Electric Cystometric Table Repackers
       - Electric Cystometric Table Relabelers
       - Electric Cystometric Table Exporters
       - Electric Cystometric Table Importers
For more information about Electric Cystometric Table 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.
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