Third Party Review Guidance for Phacofragmentation System Device Premarket Notification (510(k))

Name: Third Party Review Guidance for Phacofragmentation System Device Premarket Notification (510(k))
Creator: Food and Drug Administration
Keywords: 510k,guidances,notification,phacofragmentation,pre-market,pre-market-notification,review

Information

Type

Guidance

Regulated products

Medical Devices

Published

January 31, 1997

Last updated

March 18, 2020

Description

This document is a guidance document titled "Third Party Review Guidance for Phacofragmentation System Device Premarket Notification (510(k))".

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

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1 Main file

Third Party Review Guidance for Phacofragmentation System Device Premarket Notification (510(k))

Updated on March 18, 2020

pdf (149.0KB)

URL: https://www.fda.gov/media/72212/download
Permalink: https://data.openrid.co/en/datasets/r/e5ea7a2a-5f38-4c37-8345-5f3f6fce0868
MIME Type: application/pdf

Created on: January 31, 1997
Modified on: March 18, 2020

Size: 149.0KB

Third Party Review Guidance for Phacofragmentation System Device Premarket Notification (510(k))

Information

Type

Regulated products

Published

Last updated

Description

Tags

Organization

Country / Region

License

Feedback

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