Intravascular Administration Sets Premarket Notification Submissions [510(k)]: Guidance for Industry and FDA Staff

Name: Intravascular Administration Sets Premarket Notification Submissions [510(k)]: Guidance for Industry and FDA Staff
Creator: Food and Drug Administration
Keywords: 510k,fda,guidances,industry,intravascular,notification,pre-market,pre-market-notification,submissions

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Premarket

Published

July 11, 2008

Last updated

March 20, 2020

Description

This document provides guidance for industry and FDA staff on premarket notification submissions for intravascular administration sets.

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

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1 Main file

Intravascular Administration Sets Premarket Notification Submissions [510(k)]: Guidance for Industry and FDA Staff

Updated on March 20, 2020

pdf (317.0KB)

URL: https://www.fda.gov/media/71046/download
Permalink: https://data.openrid.co/en/datasets/r/fa8ae66b-d158-4ad0-a668-df7e1f2f3c4f
MIME Type: application/pdf

Created on: July 11, 2008
Modified on: March 20, 2020

Size: 317.0KB

Intravascular Administration Sets Premarket Notification Submissions [510(k)]: Guidance for Industry and FDA Staff

Information

Type

Regulated products

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Published

Last updated

Description

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