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FDA 510(k)

STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE

K-Number: K001961 · 2001-01-25

ApplicantStoeckert Instrumente
Decision Date2001-01-25
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE is the device name listed in this FDA 510(k) record. The listed applicant is Stoeckert Instrumente. It received FDA 510(k) clearance on 2001-01-25 under 510(k) number K001961. 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 A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE?

STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE is a medical device that received FDA 510(k) clearance on 2001-01-25. The listed applicant is Stoeckert Instrumente. The 510(k) number is K001961.

When did STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE receive FDA 510(k) clearance?

STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE received FDA 510(k) clearance on 2001-01-25, under 510(k) number K001961.

Who is the listed applicant for STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE?

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

What is the FDA product code for STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE?

The FDA product code for STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE is DWF.

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Other records listing Stoeckert Instrumente 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.

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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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