Clearance Summary
MOLDEYE received FDA 510(k) clearance under submission number K772168, sponsored by Robert B. Scott Ocularists of Florida, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1977-11-30.
- Submission: K772168
- Applicant / Sponsor: Robert B. Scott Ocularists of Florida, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.3130
- Decision date: 1977-11-30
Classification & Regulation
This clearance is catalogued under FDA product code HQN and 21 CFR 886.3130, within the Ophthalmic review panel as a Class II device.