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BIOLOGIC-DT SYSTEM

K953751 Class II Traditional
Decision Date
1996-02-15
Sponsor / Applicant
Hemocleanse, Inc.

Technical Specification

510(k) Submission ID K953751
Product Code FLD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5870
Decision Date 1996-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOLOGIC-DT SYSTEM received FDA 510(k) clearance under submission number K953751, sponsored by Hemocleanse, 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 1996-02-15.

Classification & Regulation

This clearance is catalogued under FDA product code FLD and 21 CFR 876.5870, within the Gastroenterology, Urology review panel as a Class II device.