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STATIC VESSEL ANALYZER

K082196 Class II Traditional
Decision Date
2009-06-16
Sponsor / Applicant
Imedos GmbH

Technical Specification

510(k) Submission ID K082196
Product Code HKI
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1120
Decision Date 2009-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STATIC VESSEL ANALYZER received FDA 510(k) clearance under submission number K082196, sponsored by Imedos GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2009-06-16.

Classification & Regulation

This clearance is catalogued under FDA product code HKI and 21 CFR 886.1120, within the Ophthalmic review panel as a Class II device.