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 the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2020-02-04 under 510(k) 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. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K191532.

When did The Caterpillar and Caterpillar Micro Arterial Embolization Devices receive FDA 510(k) clearance?

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

Who is the listed applicant for The Caterpillar and Caterpillar Micro Arterial Embolization Devices?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.