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U.S. FDA Medical Device Subungual Hematoma Drill Requirements


FDA Medical Device Definition: Surgical instrument motors and accessories are AC-powered, battery-powered, or air-powered devices intended for use during surgical procedures to provide power to operate various accessories or attachments to cut hard tissue or bone and soft tissue. Accessories or attachments may include a bur, chisel (osteotome), dermabrasion brush, dermatome, drill bit, hammerhead, pin driver, and saw blade.

Registrar Corp assists Subungual Hematoma Drill companies with:

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