We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Eyelid Devices Need 510(k) Notices, FDA Rules
Eyelid Devices Need 510(k) Notices, FDA Rules
August 26, 2011
Acting on a petition by TearScience for its Lipiflow device, the FDA moved eyelid thermal pulsation systems from Class III to Class II with special controls.