meddevicedb.com FDA Device Reference

D.O.R.C. HARMONY TOTAL VITRECTOMY SYSTEM

K983797 Class II Traditional
Decision Date
1999-03-03
Sponsor / Applicant
Dutch Ophthalmic USA, Inc.

Technical Specification

510(k) Submission ID K983797
Product Code HQE
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4150
Decision Date 1999-03-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

D.O.R.C. HARMONY TOTAL VITRECTOMY SYSTEM received FDA 510(k) clearance under submission number K983797, sponsored by Dutch Ophthalmic USA, 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 1999-03-03.

Classification & Regulation

This clearance is catalogued under FDA product code HQE and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.