meddevicedb.com FDA Device Reference

MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB

K022716 Class I Traditional
Decision Date
2002-10-11
Sponsor / Applicant
Med-Logics, Inc.

Technical Specification

510(k) Submission ID K022716
Product Code HNO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4370
Decision Date 2002-10-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB received FDA 510(k) clearance under submission number K022716, 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 2002-10-11.

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.