Clearance Summary
KERATOME received FDA 510(k) clearance under submission number K903912, sponsored by Micro Precision Instrument 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 1990-10-17.
- Submission: K903912
- Applicant / Sponsor: Micro Precision Instrument Co.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4370
- Decision date: 1990-10-17
Classification & Regulation
This clearance is catalogued under FDA product code HNO and 21 CFR 886.4370, within the Ophthalmic review panel as a Class I device.