meddevicedb.com FDA Device Reference

DRAINAGE WICK; SURGICAL SPEARS AND SPONGES, CORNEAL LIGHT SHIELD, INSTRUMENT WIPE

K990671 Class II Traditional
Decision Date
1999-05-10
Sponsor / Applicant
Hurricane Medical

Technical Specification

510(k) Submission ID K990671
Product Code HOZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4790
Decision Date 1999-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DRAINAGE WICK; SURGICAL SPEARS AND SPONGES, CORNEAL LIGHT SHIELD, INSTRUMENT WIPE received FDA 510(k) clearance under submission number K990671, sponsored by Hurricane Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1999-05-10.

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.