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ELECTRIC I/V POLE OR EIVP2

K935003 Class I Traditional
Decision Date
1994-01-25
Sponsor / Applicant
Optical Micro Systems, Inc.

Technical Specification

510(k) Submission ID K935003
Product Code KYG
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4360
Decision Date 1994-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRIC I/V POLE OR EIVP2 received FDA 510(k) clearance under submission number K935003, sponsored by Optical Micro Systems, 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 1994-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code KYG and 21 CFR 886.4360, within the Ophthalmic review panel as a Class I device.