CTS MIDCAB CORONARY SHUNT
K-Number: K963503 · 1997-04-03
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Device Summary
Frequently Asked Questions
What is the CTS MIDCAB CORONARY SHUNT?
CTS MIDCAB CORONARY SHUNT is a medical device that received FDA 510(k) clearance on 1997-04-03. The listed applicant is Cardiothoracic Systems, Inc.. The 510(k) number is K963503.
When did CTS MIDCAB CORONARY SHUNT receive FDA 510(k) clearance?
CTS MIDCAB CORONARY SHUNT received FDA 510(k) clearance on 1997-04-03, under 510(k) number K963503.
Who is the listed applicant for CTS MIDCAB CORONARY SHUNT?
The FDA 510(k) record lists Cardiothoracic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CTS MIDCAB CORONARY SHUNT?
The FDA product code for CTS MIDCAB CORONARY SHUNT is DXC.
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 Cardiothoracic Systems, 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.
Related Devices (Code: DXC)
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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