# Coronary and Carotid Embolic Protection Devices - Premarket Notification [510(k)] Submissions :  Guidance for Industry and FDA Staff - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/coronary-and-carotid-embolic-protection-devices-premarket-notification-510k-submissions-guidance-for-industry-and-fda-staff/a5ecf116-4c3e-4916-bee4-c75880dabd02

> FDA guidance document: Coronary and Carotid Embolic Protection Devices - Premarket Notification [510(k)] Submissions :  Guidance for Industry and FDA Staff. Issue date: February 15, 2008. Get complete insights and analysis.

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## Details

- Title: Coronary and Carotid Embolic Protection Devices - Premarket Notification [510(k)] Submissions :  Guidance for Industry and FDA Staff
- Communication Type: Guidance Document
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Office URL: /offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
- Issue Date: 2008-02-15
- Last Changed: 2020-03-20
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2020-D-0957">FDA-2020-D-0957</a>

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