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FDA 510(k)

CARBOMEDICS MITRAL ROTATOR

K-Number: K960923 · 1996-04-29

Decision Date1996-04-29
Product CodeMOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARBOMEDICS MITRAL ROTATOR is the device name listed in this FDA 510(k) record. The listed applicant is Carbomedics, Inc.. It received FDA 510(k) clearance on 1996-04-29 under 510(k) number K960923. The device is classified under product code MOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 22 devices →

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

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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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