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510(k) K020571

STOCKERT CENTRIFUGAL PUMP CONSOLE by Stockert Instrumente GmbH — Product Code DTQ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 23, 2002
Date Received
February 21, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Console, Heart-Lung Machine, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4220
Review Panel
CV
Submission Type

Other clearances by Stockert Instrumente GmbH

  • K042374 — STOCKERT SCP RHYTHM (September 23, 2004)
  • K041558 — STOCKERTIR PURGE CONTROL (APC) SYSTEM (July 2, 2004)
  • K032213 — STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP (August 29, 2003)
  • K023622 — STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35 (November 21, 2002)
  • K022280 — STOCKERT CORONARY PERFUSION CANNULAE (October 11, 2002)
  • K022321 — STOCKERT V172-28 VENOUS FEMORAL CANNULA (October 9, 2002)
  • K011838 — CENTRIFUGAL PUMP (February 5, 2002)
  • K011088 — SIII ALARM AMPLIFIER (May 2, 2001)

Other clearances for product code DTQ

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  • K221895 — Terumo Advanced Perfusion System 1 (April 18, 2023)
  • K221373 — Essenz HLM (March 9, 2023)
  • K210130 — Stockert S5 System (April 5, 2021)
  • K202125 — Century Perfusion System (March 7, 2021)
  • K190282 — Quantum Smart Occluder LH (left-hand), Quantum Smart Occluder LH (right-hand) (May 24, 2019)
  • K173834 — Quantum Pump Console (May 25, 2018)
  • K172220 — Advanced Perfusion System 1 (August 17, 2017)
  • K163531 — Advanced Perfusion System 1 (June 7, 2017)
  • K153376 — Advanced Perfusion System 1 (December 16, 2015)