Clearance Summary
OCUTOME MODEL 8000 received FDA 510(k) clearance under submission number K791898, sponsored by Cooper Medical Devices Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1979-10-30.
- Submission: K791898
- Applicant / Sponsor: Cooper Medical Devices Corp.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4150
- Decision date: 1979-10-30
Classification & Regulation
This clearance is catalogued under FDA product code HKP and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.