Registrar Corp

HomeMedical DevicesRegistration & Medical Device ListingsMedical Device Samples › U.S. FDA Tonsil Guillotine Regulations

U.S. FDA Medical Device Tonsil Guillotine Requirements

FDA Medical Device Definition: An ear, nose, and throat manual surgical instrument is one of a variety of devices intended for use in surgical procedures to examine or treat the bronchus, esophagus, trachea, larynx, pharynx, nasal and paranasal sinus, or ear. This generic type of device includes the esophageal dilator; tracheal bistour (a long, narrow surgical knife); tracheal dilator; tracheal hook; laryngeal injection set; laryngeal knife; laryngeal saw; laryngeal trocar; laryngectomy tube; adenoid curette; adenotome; metal tongue depressor; mouth gag; oral screw; salpingeal curette; tonsillectome; tonsil guillotine; tonsil screw; tonsil snare; tonsil suction tube; tonsil suturing hook; antom reforator; ethmoid curette; frontal sinus-rasp; nasal curette; nasal rasp; nasal rongeur; nasal saw; nasal scissors; nasal snare; sinus irrigator; sinus trephine; ear curette; ear excavator; ear rasp; ear scissor, ear snare; ear spoon; ear suction tube; malleous ripper; mastoid gauge; microsurgical ear chisel; myringotomy tube inserter; ossici holding clamp; sacculotomy tack inserter; vein press; wire ear loop; microrule; mirror; mobilizer; ear, nose, and throat punch; ear, nose and throat knife; and ear, nose, and throat trocar.

Registrar Corp assists Tonsil Guillotine companies with:

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