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ISCIENCE INTERVENTIONAL OPHTHALMIC MICROCATHETER

K080067 Class II Traditional
Decision Date
2008-07-18
Sponsor / Applicant
Iscience Interventional

Technical Specification

510(k) Submission ID K080067
Product Code MPA
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2008-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ISCIENCE INTERVENTIONAL OPHTHALMIC MICROCATHETER received FDA 510(k) clearance under submission number K080067, sponsored by Iscience Interventional. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2008-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code MPA and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.