meddevicedb.com FDA Device Reference

Insulin Syringes

K242434 Class II Special
Decision Date
2024-12-24
Sponsor / Applicant
Chirana T. Injecta

Technical Specification

510(k) Submission ID K242434
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2024-12-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Insulin Syringes received FDA 510(k) clearance under submission number K242434, sponsored by Chirana T. Injecta. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2024-12-24.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.