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FDA 510(k)

MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C

K-Number: K052372 · 2005-09-22

Decision Date2005-09-22
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C 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 2005-09-22 under 510(k) number K052372. 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 MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C?

MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C is a medical device that received FDA 510(k) clearance on 2005-09-22. The listed applicant is Medtronic Perfusion Systems. The 510(k) number is K052372.

When did MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C receive FDA 510(k) clearance?

MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C received FDA 510(k) clearance on 2005-09-22, under 510(k) number K052372.

Who is the listed applicant for MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C?

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 MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C?

The FDA product code for MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C is DWF.

Related Clinical Trials

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.

Other records listing Medtronic Perfusion Systems 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.

Official Source

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

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