Clearance Summary
OBF MODEL 112 VACUUM CUP SYSTEM received FDA 510(k) clearance under submission number K864959, sponsored by Ocular Blood Flow Laboratories, 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 1987-02-12.
- Submission: K864959
- Applicant / Sponsor: Ocular Blood Flow Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1930
- Decision date: 1987-02-12
Classification & Regulation
This clearance is catalogued under FDA product code HKX and 21 CFR 886.1930, within the Ophthalmic review panel as a Class II device.