U.S. FDA Medical Device Microscope Slides Requirements
FDA Medical Device Definition: Tissue processing equipment consists of devices used to prepare human tissue specimens for diagnostic histological examination by processing specimens through the various stages of decalcifying, infiltrating, sectioning, and mounting on microscope slides.
FDA Microscope Slides Label Requirements and Exceptions
FDA Microscope Slides Import Information
FDA Microscope Slides Detentions (Microscope Slides Entry Refusals)
General U.S. Food and Drug Administration Medical Device Guidelines for:
- Microscope Slides Manufacturers (Microscope Slides Suppliers)
- Microscope Slides Distributors
- Microscope Slides Processors
- Microscope Slides Repackers
- Microscope Slides Relabelers
- Microscope Slides Exporters
- Microscope Slides Importers
For more information about Microscope Slides 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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