The Caterpillar and Caterpillar Micro Arterial Embolization Devices
K-Number: K191532 · 2020-02-04
Device Summary
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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