Clearance Summary
BAUSCH & LOMB VERTOMETER V-5 received FDA 510(k) clearance under submission number K862518, 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 1986-08-11.
- Submission: K862518
- Applicant / Sponsor: Bausch & Lomb, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.1425
- Decision date: 1986-08-11
Classification & Regulation
This clearance is catalogued under FDA product code HLM and 21 CFR 886.1425, within the Ophthalmic review panel as a Class I device.