meddevicedb.com FDA Device Reference

BOBES SLIT LAMP

K945445 Class II Traditional
Decision Date
1995-10-17
Sponsor / Applicant
Bobes S.A.

Technical Specification

510(k) Submission ID K945445
Product Code HJO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1850
Decision Date 1995-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BOBES SLIT LAMP received FDA 510(k) clearance under submission number K945445, sponsored by Bobes S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1995-10-17.

Classification & Regulation

This clearance is catalogued under FDA product code HJO and 21 CFR 886.1850, within the Ophthalmic review panel as a Class II device.