meddevicedb.com FDA Device Reference

SOLOS EYESITE CAP SLEEVE

K872611 Class II Traditional
Decision Date
1987-08-10
Sponsor / Applicant
Solos Ophthalmology

Technical Specification

510(k) Submission ID K872611
Product Code HQC
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4670
Decision Date 1987-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOLOS EYESITE CAP SLEEVE received FDA 510(k) clearance under submission number K872611, sponsored by Solos Ophthalmology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1987-08-10.

Classification & Regulation

This clearance is catalogued under FDA product code HQC and 21 CFR 886.4670, within the Ophthalmic review panel as a Class II device.