Aqueous Shunts - 510(k) Submissions - Guidance for Industry and for FDA Reviewers/Staff

Name: Aqueous Shunts - 510(k) Submissions - Guidance for Industry and for FDA Reviewers/Staff
Creator: Food and Drug Administration
Keywords: 510k,fda,guidances,industry,pre-market,reviewer,submissions

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Premarket

Published

November 15, 1998

Last updated

March 18, 2020

Description

A guidance document for FDA reviewers and staff on 510(k) submissions for aqueous shunts, focusing on premarket topics.

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

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1 Main file

Aqueous Shunts - 510(k) Submissions - Guidance for Industry and for FDA Reviewers/Staff

Updated on March 18, 2020

pdf (57.2KB)

URL: https://www.fda.gov/media/71885/download
Permalink: https://data.openrid.co/en/datasets/r/9634acc5-ee3e-4a03-980e-196b71c36407
MIME Type: application/pdf

Created on: November 15, 1998
Modified on: March 18, 2020

Size: 57.2KB

Aqueous Shunts - 510(k) Submissions - Guidance for Industry and for FDA Reviewers/Staff

Information

Type

Regulated products

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Published

Last updated

Description

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Country / Region

License

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