U.S. FDA Medical Device Pocket Battery Boxes Requirements
FDA Medical Device Definition: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
FDA Pocket Battery Boxes Establishment Registration
FDA Pocket Battery Boxes Listing
FDA Pocket Battery Boxes Label Requirements and Exceptions
FDA Pocket Battery Boxes Import Information
FDA Pocket Battery Boxes Detentions (Pocket Battery Boxes Entry Refusals)
General U.S. Food and Drug Administration Medical Device Guidelines for:
- Pocket Battery Boxes Manufacturers (Pocket Battery Boxes Suppliers)
- Pocket Battery Boxes Distributors
- Pocket Battery Boxes Processors
- Pocket Battery Boxes Repackers
- Pocket Battery Boxes Relabelers
- Pocket Battery Boxes Exporters
- Pocket Battery Boxes Importers
For more information about Pocket Battery Boxes Medical Devices, simply click below:
U.S. FDA Regulations:
U.S. FDA 510(k) Regulation: 21 C.F.R. section 814.9.
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