meddevicedb.com FDA Device Reference

(BRAND NAME)

K971384 Class I Traditional
Decision Date
1997-07-01
Sponsor / Applicant
Long IN Time Ent. Co., Ltd.

Technical Specification

510(k) Submission ID K971384
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1997-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

(BRAND NAME) received FDA 510(k) clearance under submission number K971384, sponsored by Long IN Time Ent. Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1997-07-01.

Classification & Regulation

This clearance is catalogued under FDA product code HQY and 21 CFR 886.5850, within the Ophthalmic review panel as a Class I device.