Clearance Summary
FEMTO LDV Z8 Surgical Laser received FDA 510(k) clearance under submission number K150323, sponsored by Sie Ag,Surgical Instrument Engineering. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2015-10-23.
- Submission: K150323
- Applicant / Sponsor: Sie Ag,Surgical Instrument Engineering
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4390
- Decision date: 2015-10-23
Classification & Regulation
This clearance is catalogued under FDA product code OOE and 21 CFR 886.4390, within the Ophthalmic review panel as a Class II device.