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ABBOTT GLOBE HOLDER

K832911 Class II Traditional
Decision Date
1983-09-29
Sponsor / Applicant
Miami Eye Technology, Inc.

Technical Specification

510(k) Submission ID K832911
Product Code HJO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1850
Decision Date 1983-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABBOTT GLOBE HOLDER received FDA 510(k) clearance under submission number K832911, sponsored by Miami Eye Technology, 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 1983-09-29.

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.