meddevicedb.com FDA Device Reference

AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water

K181814 Class II Traditional
Decision Date
2018-09-04
Sponsor / Applicant
Amsino International, Inc.

Technical Specification

510(k) Submission ID K181814
Product Code EZL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 2018-09-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water received FDA 510(k) clearance under submission number K181814, sponsored by Amsino International, Inc.. 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 2018-09-04.

Classification & Regulation

This clearance is catalogued under FDA product code EZL and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.