Clearance Summary
SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P. received FDA 510(k) clearance under submission number K875063, sponsored by Epson EL Paso, 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 1988-02-22.
- Submission: K875063
- Applicant / Sponsor: Epson EL Paso, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5844
- Decision date: 1988-02-22
Classification & Regulation
This clearance is catalogued under FDA product code HQG and 21 CFR 886.5844, within the Ophthalmic review panel as a Class I device.