CPG Sec. 300.600 Commercial Distribution with Regard to Premarket Notification (Section 510(k))

Name: CPG Sec. 300.600 Commercial Distribution with Regard to Premarket Notification (Section 510(k))
Creator: Food and Drug Administration
Keywords: 510k,compliance,distribution,guide,notification,policies,pre-market,pre-market-notification,regulations

Information

Type

Compliance Policy Guide (CPG)

Regulated products

Medical Devices

Published

September 23, 1987

Last updated

May 3, 2021

Description

CPG Sec. 300.600 outlines regulations for commercial distribution and premarket notification (Section 510(k)) in the CPG.

Organization

Food and Drug Administration (FDA) 🇺🇸

Country / Region

United States

License

Other (Public Domain)

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CPG Sec. 300.600 Commercial Distribution with Regard to Premarket Notification (Section 510(k))

Updated on May 3, 2021

none

URL: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/cpg-sec-300600-commercial-distribution-regard-premarket-notification-section-510k
Permalink: https://data.openrid.co/en/datasets/r/bee5c422-554b-403d-ba8c-53cd189077db
MIME Type: None

Created on: September 23, 1987
Modified on: May 3, 2021

CPG Sec. 300.600 Commercial Distribution with Regard to Premarket Notification (Section 510(k))

Information

Type

Regulated products

Published

Last updated

Description

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Organization

Country / Region

License

Feedback

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