Clearance Summary
KEELER MULTILASE 3000 received FDA 510(k) clearance under submission number K942180, sponsored by Keeler Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1994-11-22.
- Submission: K942180
- Applicant / Sponsor: Keeler Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4390
- Decision date: 1994-11-22
Classification & Regulation
This clearance is catalogued under FDA product code HQF and 21 CFR 886.4390, within the Ophthalmic review panel as a Class II device.