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PASSPORT FOLDABLE LENS PLACEMENT SYSTEM

K951292 Class I Traditional
Decision Date
1995-06-02
Sponsor / Applicant
Chiron Vision Corp.

Technical Specification

510(k) Submission ID K951292
Product Code KYB
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4300
Decision Date 1995-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PASSPORT FOLDABLE LENS PLACEMENT SYSTEM received FDA 510(k) clearance under submission number K951292, sponsored by Chiron Vision Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1995-06-02.

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.