meddevicedb.com FDA Device Reference

Enteral Syringe (20ml, 60ml)

K252483 Class II Traditional
Decision Date
2026-07-01
Sponsor / Applicant
Chirana T.Injecta,A.S.

Technical Specification

510(k) Submission ID K252483
Product Code PNR
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2026-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Enteral Syringe (20ml, 60ml) received FDA 510(k) clearance under submission number K252483, sponsored by Chirana T.Injecta,A.S.. 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 2026-07-01.

Classification & Regulation

This clearance is catalogued under FDA product code PNR and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.