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FF450 PLUS FUNDUS CAMERA AND VISUPAC DIGITAL IMAGE ARCHIVING SYSTEM, OR FF450 PLUS VISUPAC SYSTEM

K011877 Class II Traditional
Decision Date
2001-09-26
Sponsor / Applicant
Carl Zeiss Jena GmbH

Technical Specification

510(k) Submission ID K011877
Product Code HKI
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1120
Decision Date 2001-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FF450 PLUS FUNDUS CAMERA AND VISUPAC DIGITAL IMAGE ARCHIVING SYSTEM, OR FF450 PLUS VISUPAC SYSTEM received FDA 510(k) clearance under submission number K011877, sponsored by Carl Zeiss Jena GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2001-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code HKI and 21 CFR 886.1120, within the Ophthalmic review panel as a Class II device.