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U.S. FDA Medical Device Tumor Localization Needle Requirements


FDA Medical Device Definition: A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.

Registrar Corp assists Tumor Localization Needle companies with:

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