BIOLOGIC DT-1000 MACHINE— 510(k) K923046

Name: FDA 510(k) clearance K923046
Creator: U.S. Food and Drug Administration
Published: 1994-09-30

Substantially Equivalent

Hemocleanse, Inc.

FDA 510(k) clearance K923046 for BIOLOGIC DT-1000 MACHINE, Substantially Equivalent on 1994-09-30. Applicant: Hemocleanse, Inc.. Device class: 2.

Clearance details

Applicant: Hemocleanse, Inc.
Product code: Code KNT
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1992-06-24
Decision date: 1994-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Lafayette, IN, US

Download summary PDF View on FDA.gov ↗

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K993330 — THERMOCHEM-HT SYSTEM1999-12-30
K992196 — BIOLOGIC-DT SYSTEM (BIOLOGIC-DT-1000 WITH DT-1000-TK)1999-09-10
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Adverse events under product code KNT

product code KNT

Death: 192
Injury: 6,034
Malfunction: 4,049
Other: 1
Total: 10,276

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.