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FDA 510(k)

STOCKERT V172-28 VENOUS FEMORAL CANNULA

K-Number: K022321 · 2002-10-09

ApplicantStockert Instrumente GmbH
Decision Date2002-10-09
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT V172-28 VENOUS FEMORAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Stockert Instrumente GmbH. It received FDA 510(k) clearance on 2002-10-09 under 510(k) number K022321. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOCKERT V172-28 VENOUS FEMORAL CANNULA?

STOCKERT V172-28 VENOUS FEMORAL CANNULA is a medical device that received FDA 510(k) clearance on 2002-10-09. The listed applicant is Stockert Instrumente GmbH. The 510(k) number is K022321.

When did STOCKERT V172-28 VENOUS FEMORAL CANNULA receive FDA 510(k) clearance?

STOCKERT V172-28 VENOUS FEMORAL CANNULA received FDA 510(k) clearance on 2002-10-09, under 510(k) number K022321.

Who is the listed applicant for STOCKERT V172-28 VENOUS FEMORAL CANNULA?

The FDA 510(k) record lists Stockert Instrumente GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STOCKERT V172-28 VENOUS FEMORAL CANNULA?

The FDA product code for STOCKERT V172-28 VENOUS FEMORAL CANNULA is DWF.

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Other records listing Stockert Instrumente GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K042374STOCKERT SCP RHYTHMK041558STOCKERTIR PURGE CONTROL (APC) SYSTEMK032213STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMPK023622STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35K022280STOCKERT CORONARY PERFUSION CANNULAEK020571STOCKERT CENTRIFUGAL PUMP CONSOLE

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Related Devices (Code: DWF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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