Clearance Summary
M2 SINGLE USE MICROKERTOME received FDA 510(k) clearance under submission number K022560, sponsored by Moria SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2002-09-27.
- Submission: K022560
- Applicant / Sponsor: Moria SA
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4370
- Decision date: 2002-09-27
Classification & Regulation
This clearance is catalogued under FDA product code HMY and 21 CFR 886.4370, within the Ophthalmic review panel as a Class I device.