Clearance Summary
ALTEX MODEL UST-3000E received FDA 510(k) clearance under submission number K924033, sponsored by Optro-Mechanics (Usa) 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 1992-11-05.
- Submission: K924033
- Applicant / Sponsor: Optro-Mechanics (Usa) Corp.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4670
- Decision date: 1992-11-05
Classification & Regulation
This clearance is catalogued under FDA product code HQC and 21 CFR 886.4670, within the Ophthalmic review panel as a Class II device.