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LOOK LENS LOOPS

K870440 Class I Traditional
Decision Date
1987-02-20
Sponsor / Applicant
Look, Inc.

Technical Specification

510(k) Submission ID K870440
Product Code HNQ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4350
Decision Date 1987-02-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LOOK LENS LOOPS received FDA 510(k) clearance under submission number K870440, sponsored by Look, 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 1987-02-20.

Classification & Regulation

This clearance is catalogued under FDA product code HNQ and 21 CFR 886.4350, within the Ophthalmic review panel as a Class I device.