# Premarket Studies of Implantable Minimally Invasive Glaucoma Surgical (MIGS) Devices: Guidance for Industry and Food and Drug Administration Staff - FDA Guidance Document Source: https://www.globalkeysolutions.net/guidances/guidance-document/premarket-studies-of-implantable-minimally-invasive-glaucoma-surgical-migs-devices-guidance-for-industry-and-food-and-drug-administration-staff/0dddd7a4-66f5-4a37-a281-f96722b7a67a > FDA guidance document: Premarket Studies of Implantable Minimally Invasive Glaucoma Surgical (MIGS) Devices: Guidance for Industry and Food and Drug Administration Staff. Issue date: December 15, 2015. Get complete insights and analysis. --- ## Details - Title: Premarket Studies of Implantable Minimally Invasive Glaucoma Surgical (MIGS) Devices: Guidance for Industry and Food and Drug Administration 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: 2015-12-15 - Comment Close Date: 2015-05-12 - Last Changed: 2020-03-02 - Docket Number: FDA-2015-D-0288 ## Related Documents - [Premarket Notification Requirements Concerning Gowns Intended for Use in Health Care Settings: Guidance for Industry and Food and Drug Administration Staff](https://www.globalkeysolutions.net/guidances/guidance-document/premarket-notification-requirements-concerning-gowns-intended-for-use-in-health-care-settings-guidance-for-industry-and-food-and-drug-administration-staff/c5e87407-606e-4a6d-bbff-36b19acebe1c) - [Endotoxin Testing Recommendations for Single-Use Intraocular Ophthalmic Devices](https://www.globalkeysolutions.net/guidances/guidance-document/endotoxin-testing-recommendations-for-single-use-intraocular-ophthalmic-devices/634c9890-4791-491a-a0dc-5692d9e03615) - [Replacement Reagent and Instrument Family Policy for In Vitro Diagnostic Devices: Guidance for Industry and FDA Staff](https://www.globalkeysolutions.net/guidances/guidance-document/replacement-reagent-and-instrument-family-policy-for-in-vitro-diagnostic-devices-guidance-for-industry-and-fda-staff/6acf5cea-4730-4835-bf2d-eb7474c6d3e6)