meddevicedb.com FDA Device Reference

HemoCare Bicarbonate Concentrate Set (BCS)

K240920 Class II Traditional
Decision Date
2024-07-12
Sponsor / Applicant
Deka Research and Development

Technical Specification

510(k) Submission ID K240920
Product Code KPO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 2024-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HemoCare Bicarbonate Concentrate Set (BCS) received FDA 510(k) clearance under submission number K240920, sponsored by Deka Research and Development. 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 2024-07-12.

Classification & Regulation

This clearance is catalogued under FDA product code KPO and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.