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MEDLOGICS ML 4000, MODEL 4000

K002515 Class I Traditional
Decision Date
2001-02-22
Sponsor / Applicant
Med-Logics, Inc.

Technical Specification

510(k) Submission ID K002515
Product Code HNO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4370
Decision Date 2001-02-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDLOGICS ML 4000, MODEL 4000 received FDA 510(k) clearance under submission number K002515, sponsored by Med-Logics, 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 2001-02-22.

Classification & Regulation

This clearance is catalogued under FDA product code HNO and 21 CFR 886.4370, within the Ophthalmic review panel as a Class I device.