meddevicedb.com FDA Device Reference

DISPOSABLE ASPIRATION NEEDLE NA-200H

K023272 Class II Traditional
Decision Date
2002-12-23
Sponsor / Applicant
The Olympus Optical Co.

Technical Specification

510(k) Submission ID K023272
Product Code FCG
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 2002-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE ASPIRATION NEEDLE NA-200H received FDA 510(k) clearance under submission number K023272, sponsored by The Olympus Optical Co.. 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 2002-12-23.

Classification & Regulation

This clearance is catalogued under FDA product code FCG and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.