FDA 510(k)

BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT

K-Number: K052524 · 2005-11-22

Decision Date2005-11-22

Product CodeDWF

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Perfusion Systems. It received FDA 510(k) clearance on 2005-11-22 under 510(k) number K052524. 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 BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT?

BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT is a medical device that received FDA 510(k) clearance on 2005-11-22. The listed applicant is Medtronic Perfusion Systems. The 510(k) number is K052524.

When did BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT receive FDA 510(k) clearance?

BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT received FDA 510(k) clearance on 2005-11-22, under 510(k) number K052524.

Who is the listed applicant for BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT?

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

What is the FDA product code for BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT?

The FDA product code for BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT is DWF.

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Related Devices (Code: DWF)

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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.