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FDA 510(k)

CARDIO VISION MICS AORTIC CLAMPS

K-Number: K123571 · 2013-08-01

ApplicantCardiomedical GmbH
Decision Date2013-08-01
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIO VISION MICS AORTIC CLAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Cardiomedical GmbH. It received FDA 510(k) clearance on 2013-08-01 under 510(k) number K123571. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIO VISION MICS AORTIC CLAMPS?

CARDIO VISION MICS AORTIC CLAMPS is a medical device that received FDA 510(k) clearance on 2013-08-01. The listed applicant is Cardiomedical GmbH. The 510(k) number is K123571.

When did CARDIO VISION MICS AORTIC CLAMPS receive FDA 510(k) clearance?

CARDIO VISION MICS AORTIC CLAMPS received FDA 510(k) clearance on 2013-08-01, under 510(k) number K123571.

Who is the listed applicant for CARDIO VISION MICS AORTIC CLAMPS?

The FDA 510(k) record lists Cardiomedical GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARDIO VISION MICS AORTIC CLAMPS?

The FDA product code for CARDIO VISION MICS AORTIC CLAMPS is DXC.

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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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