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FDA 510(k)

DeRoyal Angiography Kits

K-Number: K152978 · 2016-03-25

Decision Date2016-03-25
Product CodeDXT
Advisory CommitteeCV
DecisionUnknown

Device Summary

DeRoyal Angiography Kits is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 2016-03-25 under 510(k) number K152978. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DeRoyal Angiography Kits?

DeRoyal Angiography Kits is a medical device that received FDA 510(k) clearance on 2016-03-25. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K152978.

When did DeRoyal Angiography Kits receive FDA 510(k) clearance?

DeRoyal Angiography Kits received FDA 510(k) clearance on 2016-03-25, under 510(k) number K152978.

Who is the listed applicant for DeRoyal Angiography Kits?

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

What is the FDA product code for DeRoyal Angiography Kits?

The FDA product code for DeRoyal Angiography Kits is DXT.

Other records listing Deroyal Industries, 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.

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Related Devices (Code: DXT)

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.