Clearance Summary
BURTON KERATOMETER - MODLE 2040 received FDA 510(k) clearance under submission number K924779, sponsored by R.H. Burton Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1993-04-05.
- Submission: K924779
- Applicant / Sponsor: R.H. Burton Co.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.1450
- Decision date: 1993-04-05
Classification & Regulation
This clearance is catalogued under FDA product code HJB and 21 CFR 886.1450, within the Ophthalmic review panel as a Class I device.