Clearance Summary
PHOTRON VISUAL FIELD ANALYZER received FDA 510(k) clearance under submission number K860642, sponsored by Biosan Laboratories, 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 1986-04-15.
- Submission: K860642
- Applicant / Sponsor: Biosan Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.1810
- Decision date: 1986-04-15
Classification & Regulation
This clearance is catalogued under FDA product code HOM and 21 CFR 886.1810, within the Ophthalmic review panel as a Class I device.