# Third Party Review Guidance For Vitreous Aspiration and Cutting Device Premarket Notification (510(k)) - FDA Guidance Document

Source: https://www.keypedia.com/guidances/guidance-document/third-party-review-guidance-for-vitreous-aspiration-and-cutting-device-premarket-notification-510k/49a8b1be-5823-4c6e-bc2c-1109bce662bd

> FDA guidance document: Third Party Review Guidance For Vitreous Aspiration and Cutting Device Premarket Notification (510(k)). Issue date: January 30, 1997. Get complete insights and analysis.

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## Details

- Title: Third Party Review Guidance For Vitreous Aspiration and Cutting Device Premarket Notification (510(k))
- Communication Type: Guidance Document
- Product Type: Medical Devices
- Office Name: Center for Devices and Radiological Health
- Issue Date: 1997-01-30
- Docket Number: FDA-2020-D-0957

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