Clearance Summary
BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR received FDA 510(k) clearance under submission number K862519, sponsored by Bausch & Lomb, 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 1986-07-23.
- Submission: K862519
- Applicant / Sponsor: Bausch & Lomb, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.1680
- Decision date: 1986-07-23
Classification & Regulation
This clearance is catalogued under FDA product code HOS and 21 CFR 886.1680, within the Ophthalmic review panel as a Class I device.