MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C
K-Number: K052372 · 2005-09-22
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Device Summary
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.
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
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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