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FDA 510(k)

RESUBMITTED MULTIORGAN PERFUSION CANNULA

K-Number: K902394 · 1990-09-27

ApplicantFresenius USA, Inc.
Decision Date1990-09-27
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RESUBMITTED MULTIORGAN PERFUSION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius USA, Inc.. It received FDA 510(k) clearance on 1990-09-27 under 510(k) number K902394. 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 RESUBMITTED MULTIORGAN PERFUSION CANNULA?

RESUBMITTED MULTIORGAN PERFUSION CANNULA is a medical device that received FDA 510(k) clearance on 1990-09-27. The listed applicant is Fresenius USA, Inc.. The 510(k) number is K902394.

When did RESUBMITTED MULTIORGAN PERFUSION CANNULA receive FDA 510(k) clearance?

RESUBMITTED MULTIORGAN PERFUSION CANNULA received FDA 510(k) clearance on 1990-09-27, under 510(k) number K902394.

Who is the listed applicant for RESUBMITTED MULTIORGAN PERFUSION CANNULA?

The FDA 510(k) record lists Fresenius USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESUBMITTED MULTIORGAN PERFUSION CANNULA?

The FDA product code for RESUBMITTED MULTIORGAN PERFUSION CANNULA is DWF.

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Other records listing Fresenius USA, Inc. 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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