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FDA 510(k)

The Caterpillar and Caterpillar Micro Arterial Embolization Devices

K-Number: K191532 · 2020-02-04

Decision Date2020-02-04
Product CodeKRD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

The Caterpillar and Caterpillar Micro Arterial Embolization Devices is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2020-02-04 under approval number K191532. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the The Caterpillar and Caterpillar Micro Arterial Embolization Devices?

The Caterpillar and Caterpillar Micro Arterial Embolization Devices is a medical device that received FDA 510(k) clearance on 2020-02-04. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K191532.

When was The Caterpillar and Caterpillar Micro Arterial Embolization Devices approved by the FDA?

The Caterpillar and Caterpillar Micro Arterial Embolization Devices received FDA 510(k) clearance on 2020-02-04, under approval number K191532.

What company makes The Caterpillar and Caterpillar Micro Arterial Embolization Devices?

The Caterpillar and Caterpillar Micro Arterial Embolization Devices is manufactured by C.R. Bard, Inc..

What is the FDA product code for The Caterpillar and Caterpillar Micro Arterial Embolization Devices?

The FDA product code for The Caterpillar and Caterpillar Micro Arterial Embolization Devices is KRD.

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Official Source

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