FDA 21 CFR Part 872 Dental Devices

FDA 21 CFR Part 872 Dental Devices

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Table of contents

Subpart A - General Provisions

872.1 Scope.

872.3 Effective dates of requirement for premarket approval.

872.9 Limitations of exemptions from section 510(k) of the Federal Food, Drug, and Cosmetic Act (the act).

Subpart B - Diagnostic Devices

872.1500 Gingival fluid measurer.

872.1720 Pulp tester.

872.1730 Electrode gel for pulp testers.

872.1740 Caries detection device.

872.1745 Laser fluorescence caries detection device.

872.1800 Extraoral source x-ray system.

872.1810 Intraoral source x-ray system.

872.1820 Dental x-ray exposure alignment device.

872.1830 Cephalometer.

872.1840 Dental x-ray position indicating device.

872.1850 Lead-lined position indicator.

872.1870 Sulfide detection device.

872.1905 Dental x-ray film holder.

872.2050 Dental sonography device.

872.2060 Jaw tracking device.

Subpart C [Reserved]

Subpart D - Prosthetic Devices

Subpart E - Surgical Devices

Subpart F - Therapeutic Devices, (and)

Subpart G - Miscellaneous Devices

FDA 21 CFR Part 872 Dental Devices:

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