Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Immersion Type Slide Stainer Regulations

U.S. FDA Medical Device Immersion Type Slide Stainer Requirements


FDA Medical Device Definition: An automated slide stainer is a device used to stain histology, cytology, and hematology slides for diagnosis.

Registrar Corp assists Immersion Type Slide Stainer companies with:

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