Clearance Summary
CLARUS ENDOSCOPIC HOOK KNIFE received FDA 510(k) clearance under submission number K925741, sponsored by Clarus Medical Systems, 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 1993-08-24.
- Submission: K925741
- Applicant / Sponsor: Clarus Medical Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1630
- Decision date: 1993-08-24
Classification & Regulation
This clearance is catalogued under FDA product code HLX and 21 CFR 886.1630, within the Ophthalmic review panel as a Class II device.