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MB 102 MILLENNIUM BLADES

K020122 Class I Traditional
Decision Date
2002-02-15
Sponsor / Applicant
Millennium Biomedical, Inc.

Technical Specification

510(k) Submission ID K020122
Product Code HNO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4370
Decision Date 2002-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MB 102 MILLENNIUM BLADES received FDA 510(k) clearance under submission number K020122, sponsored by Millennium Biomedical, 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 2002-02-15.

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.