Clearance Summary
PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM received FDA 510(k) clearance under submission number K881358, sponsored by Neuroscientific 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 1988-06-27.
- Submission: K881358
- Applicant / Sponsor: Neuroscientific Corp.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.1150
- Decision date: 1988-06-27
Classification & Regulation
This clearance is catalogued under FDA product code HOX and 21 CFR 886.1150, within the Ophthalmic review panel as a Class I device.