Guidance on the Content of Premarket Notification [510(K)] Submissions for Hypodermic Single Lumen Needles

Name: Guidance on the Content of Premarket Notification [510(K)] Submissions for Hypodermic Single Lumen Needles
Creator: Food and Drug Administration
Keywords: 510k,guidances,needles,notification,pre-market,pre-market-notification,submissions

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Premarket

Published

March 31, 1993

Last updated

March 17, 2020

Description

This document provides guidance on the content of premarket notification submissions for hypodermic single lumen needles.

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

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Guidance on the Content of Premarket Notification [510(K)] Submissions for Hypodermic Single Lumen Needles

Updated on March 17, 2020

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URL: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/guidance-content-premarket-notification-510k-submissions-hypodermic-single-lumen-needles
Permalink: https://data.openrid.co/en/datasets/r/1cbf25d0-cc87-4042-bd03-7495561e5958
MIME Type: None

Created on: March 31, 1993
Modified on: March 17, 2020

Guidance on the Content of Premarket Notification [510(K)] Submissions for Hypodermic Single Lumen Needles

Information

Type

Regulated products

Topics

Published

Last updated

Description

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Organization

Country / Region

License

Feedback

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