Medical Devices; Ophthalmic Devices; Classification of Nasolacrimal Compression Device

Information

Type

Rule

Regulated products

Medical Devices

Published

June 10, 2016

Last updated

June 10, 2016

Description

Document number 2016-13788. The Food and Drug Administration (FDA) is classifying the nasolacrimal compression device into class I (general controls). The Agency is classifying the device into class I (general controls) in order to provide a reasonable assurance of safety and effectiveness of the device.

Organization

Country / Region

United States

License

Other (Public Domain)

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