meddevicedb.com FDA Device Reference

EXPANDACELL EYE SPEAR, EYE WICK, WICK DRAIN AND CORNEAL SHIELD

K964855 Class II Traditional
Decision Date
1997-03-04
Sponsor / Applicant
Shippert Medical Technologies Corp.

Technical Specification

510(k) Submission ID K964855
Product Code HOZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4790
Decision Date 1997-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXPANDACELL EYE SPEAR, EYE WICK, WICK DRAIN AND CORNEAL SHIELD received FDA 510(k) clearance under submission number K964855, sponsored by Shippert Medical Technologies Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1997-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code HOZ and 21 CFR 886.4790, within the Ophthalmic review panel as a Class II device.