# Medical Device User Fee and Modernization Act of 2002, Validation Data in Premarket Notification Submissions (510(k)s) for Reprocessed Single-Use Medical Devices:  Guidance for Industry and FDA Staff - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/medical-device-user-fee-and-modernization-act-of-2002-validation-data-in-premarket-notification-submissions-510ks-for-reprocessed-single-use-medical-devices-guidance-for-industry-and-fda-staff/acb7ac03-f27d-4689-a580-1296d1caf05e

> FDA guidance document: Medical Device User Fee and Modernization Act of 2002, Validation Data in Premarket Notification Submissions (510(k)s) for Reprocessed Single-Use Medical Devices:  Guidance for Industry and FDA Staff. Issue date: June 02, 2004. Get complete insights and analysis.

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## Details

- Title: Medical Device User Fee and Modernization Act of 2002, Validation Data in Premarket Notification Submissions (510(k)s) for Reprocessed Single-Use Medical Devices:  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: 2004-06-02
- Last Changed: 2020-02-28
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2003-D-0309">FDA-2003-D-0309</a>

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