meddevicedb.com FDA Device Reference

DEROYAL INDUSTRIES, INC. NEONATAL EYE COVER

K962290 Class I Traditional
Decision Date
1996-07-03
Sponsor / Applicant
Debusk Technology Corp.

Technical Specification

510(k) Submission ID K962290
Product Code FOK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5270
Decision Date 1996-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEROYAL INDUSTRIES, INC. NEONATAL EYE COVER received FDA 510(k) clearance under submission number K962290, sponsored by Debusk Technology Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1996-07-03.

Classification & Regulation

This clearance is catalogued under FDA product code FOK and 21 CFR 880.5270, within the General Hospital review panel as a Class I device.