Guidance on PMA Interactive Procedures for Day-100 Meetings and Subsequent Deficiencies - for Use by CDRH and Industry

Name: Guidance on PMA Interactive Procedures for Day-100 Meetings and Subsequent Deficiencies - for Use by CDRH and Industry
Creator: Food and Drug Administration
Keywords: cdrh,center-for-devices-and-radiological-health,guidances,industry,meetings,pma,pre-market-authorization,procedures

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Administrative / Procedural, Premarket

Published

February 18, 1998

Last updated

March 18, 2020

Description

This document provides guidance on interactive procedures for day-100 meetings and subsequent deficiencies for CDRH and industry.

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

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1 Main file

Guidance on PMA Interactive Procedures for Day-100 Meetings and Subsequent Deficiencies - for Use by CDRH and Industry

Updated on March 18, 2020

pdf (12.6KB)

URL: https://www.fda.gov/media/72655/download
Permalink: https://data.openrid.co/en/datasets/r/bb5929ce-6f9a-4a0f-81c2-bda8aa263ac3
MIME Type: application/pdf

Created on: February 18, 1998
Modified on: March 18, 2020

Size: 12.6KB

Guidance on PMA Interactive Procedures for Day-100 Meetings and Subsequent Deficiencies - for Use by CDRH and Industry

Information

Type

Regulated products

Topics

Published

Last updated

Description

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Organization

Country / Region

License

Feedback

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