meddevicedb.com FDA Device Reference

PHAKOSYSTEMS MODEL 1000/OMNI PACKS IRRIGATION/ASPIRATION

K830871 Class I Traditional
Decision Date
1983-06-02
Sponsor / Applicant
Phakosystems, Inc.

Technical Specification

510(k) Submission ID K830871
Product Code HOC
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4350
Decision Date 1983-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHAKOSYSTEMS MODEL 1000/OMNI PACKS IRRIGATION/ASPIRATION received FDA 510(k) clearance under submission number K830871, sponsored by Phakosystems, 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 1983-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code HOC and 21 CFR 886.4350, within the Ophthalmic review panel as a Class I device.