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U.S. FDA Medical Device Medication Reminder Requirements

FDA Medical Device Definition: A daily activity assist device is a modified adaptor or utensil (e.g., a dressing, grooming, recreational activity, transfer, eating, or homemaking aid) that is intended for medical purposes to assist a patient to perform a specific function.

Registrar Corp assists Medication Reminder companies with:

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