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US-HOLO SUNGLASSES

K961035 Class I Traditional
Decision Date
1996-04-10
Sponsor / Applicant
Mi Technologies, Inc.

Technical Specification

510(k) Submission ID K961035
Product Code HQY
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5850
Decision Date 1996-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

US-HOLO SUNGLASSES received FDA 510(k) clearance under submission number K961035, sponsored by Mi Technologies, 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 1996-04-10.

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.