Guidance for Cardiovascular Intravascular Filter 510(k) Submissions - Guidance for Industry and FDA Staff

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Premarket

Published

November 25, 1999

Last updated

March 18, 2020

Description

This document is a guidance for industry and FDA staff on cardiovascular intravascular filter 510(k) submissions.

Organization

Country / Region

United States

License

Other (Public Domain)

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