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InjecSURE Injection System

K253598 Class II Traditional
Decision Date
2026-03-31
Sponsor / Applicant
Carbon Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K253598
Product Code FBK
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2026-03-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

InjecSURE Injection System received FDA 510(k) clearance under submission number K253598, sponsored by Carbon Medical Technologies, 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 2026-03-31.

Classification & Regulation

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