Dental Composite Resin Devices - Premarket Notification [510(k)] Submissions - Guidance for Industry and FDA Staff

Name: Dental Composite Resin Devices - Premarket Notification [510(k)] Submissions - Guidance for Industry and FDA Staff
Creator: Food and Drug Administration
Keywords: 510k,dental,fda,guidances,industry,notification,pre-market,pre-market-notification,submissions

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Premarket

Published

October 25, 2005

Last updated

March 19, 2020

Description

This document is a guidance for industry and FDA staff on premarket notification submissions for dental composite resin devices.

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

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1 Main file

Dental Composite Resin Devices - Premarket Notification [510(k)] Submissions - Guidance for Industry and FDA Staff

Updated on March 19, 2020

none

URL: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/dental-composite-resin-devices-premarket-notification-510k-submissions-guidance-industry-and-fda
Permalink: https://data.openrid.co/en/datasets/r/0bf2e8c4-1be2-47da-86fa-641a1a2b5188
MIME Type: None

Created on: October 25, 2005
Modified on: March 19, 2020

Dental Composite Resin Devices - Premarket Notification [510(k)] Submissions - Guidance for Industry and FDA Staff

Information

Type

Regulated products

Topics

Published

Last updated

Description

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Organization

Country / Region

License

Feedback

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