meddevicedb.com FDA Device Reference

DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)

K983129 Class I Traditional
Decision Date
1998-12-04
Sponsor / Applicant
Staar Surgical Co.

Technical Specification

510(k) Submission ID K983129
Product Code KYB
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4300
Decision Date 1998-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1) received FDA 510(k) clearance under submission number K983129, sponsored by Staar Surgical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1998-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code KYB and 21 CFR 886.4300, within the Ophthalmic review panel as a Class I device.