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VIT COMMANDER SYSTEM

K961738 Class II Traditional
Decision Date
1996-11-25
Sponsor / Applicant
Scieran Technologies, Inc.

Technical Specification

510(k) Submission ID K961738
Product Code HQE
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4150
Decision Date 1996-11-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VIT COMMANDER SYSTEM received FDA 510(k) clearance under submission number K961738, sponsored by Scieran Technologies, 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 1996-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code HQE and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.