Clearance Summary
STARION UNIVERSAL POWER SUPPLY received FDA 510(k) clearance under submission number K070871, sponsored by Starion Instruments. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2007-04-13.
- Submission: K070871
- Applicant / Sponsor: Starion Instruments
- Clearance pathway: Special
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4115
- Decision date: 2007-04-13
Classification & Regulation
This clearance is catalogued under FDA product code HQO and 21 CFR 886.4115, within the Ophthalmic review panel as a Class II device.