STOCKERT CENTRIFUGAL PUMP CONSOLE— 510(k) K020571

Name: FDA 510(k) clearance K020571
Creator: U.S. Food and Drug Administration
Published: 2002-09-23

Substantially Equivalent

Stockert Instrumente GmbH

FDA 510(k) clearance K020571 for STOCKERT CENTRIFUGAL PUMP CONSOLE, Substantially Equivalent on 2002-09-23. Applicant: Stockert Instrumente GmbH. Device class: 2.

Clearance details

Applicant: Stockert Instrumente GmbH
Product code: Code DTQ
Device class: Class 2
Regulation: 21 CFR 870.4220
Advisory panel: Cardiovascular
Date received: 2002-02-21
Decision date: 2002-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DTQ

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K232291 — Essenz HLM, Essenz ILBM2023-08-24
K221895 — Terumo Advanced Perfusion System 12023-04-18
K221373 — Essenz HLM2023-03-09
K210130 — Stockert S5 System2021-04-05
K202125 — Century Perfusion System2021-03-07

More clearances from Stockert Instrumente GmbH

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K042374 — STOCKERT SCP RHYTHM2004-09-23
K041558 — STOCKERTIR PURGE CONTROL (APC) SYSTEM2004-07-02
K032213 — STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP2003-08-29
K023622 — STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-352002-11-21
K022280 — STOCKERT CORONARY PERFUSION CANNULAE2002-10-11

Adverse events under product code DTQ

product code DTQ

Death: 123
Malfunction: 4,822
Other: 1
Total: 4,946

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.