Clearance Summary
DGH MODEL 9000 received FDA 510(k) clearance under submission number K965127, sponsored by Dgh Technology, 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 1997-03-17.
- Submission: K965127
- Applicant / Sponsor: Dgh Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4670
- Decision date: 1997-03-17
Classification & Regulation
This clearance is catalogued under FDA product code HQC and 21 CFR 886.4670, within the Ophthalmic review panel as a Class II device.