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U.S. FDA Medical Device Laryngectomy Tube 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 Laryngectomy Tube companies with:

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