Clearance Summary
TOMEY PE-300 PORTABLE ERG received FDA 510(k) clearance under submission number K921815, sponsored by Tomey Corporation USA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1992-07-15.
- Submission: K921815
- Applicant / Sponsor: Tomey Corporation USA
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1640
- Decision date: 1992-07-15
Classification & Regulation
This clearance is catalogued under FDA product code HLT and 21 CFR 886.1640, within the Ophthalmic review panel as a Class II device.