Clearance Summary
LASER CENTERING DEVICE received FDA 510(k) clearance under submission number K872747, sponsored by Innomed 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 1987-09-04.
- Submission: K872747
- Applicant / Sponsor: Innomed Corp.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4570
- Decision date: 1987-09-04
Classification & Regulation
This clearance is catalogued under FDA product code HMR and 21 CFR 886.4570, within the Ophthalmic review panel as a Class I device.