CARBOMEDICS MITRAL ROTATOR
K-Number: K960923 · 1996-04-29
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Device Summary
Frequently Asked Questions
What is the CARBOMEDICS MITRAL ROTATOR?
CARBOMEDICS MITRAL ROTATOR is a medical device that received FDA 510(k) clearance on 1996-04-29. The listed applicant is Carbomedics, Inc.. The 510(k) number is K960923.
When did CARBOMEDICS MITRAL ROTATOR receive FDA 510(k) clearance?
CARBOMEDICS MITRAL ROTATOR received FDA 510(k) clearance on 1996-04-29, under 510(k) number K960923.
Who is the listed applicant for CARBOMEDICS MITRAL ROTATOR?
The FDA 510(k) record lists Carbomedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARBOMEDICS MITRAL ROTATOR?
The FDA product code for CARBOMEDICS MITRAL ROTATOR is MOP.
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 Carbomedics, 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: MOP)
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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