Clearance Summary
SURGICAL KNIFE received FDA 510(k) clearance under submission number K834546, sponsored by Fine-Cut Diamond Instruments. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1984-03-16.
- Submission: K834546
- Applicant / Sponsor: Fine-Cut Diamond Instruments
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4350
- Decision date: 1984-03-16
Classification & Regulation
This clearance is catalogued under FDA product code HNN and 21 CFR 886.4350, within the Ophthalmic review panel as a Class I device.