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FDA 510(k)

DeRoyal Angiography Kits

K-Number: K152978 · 2016-03-25

ApplicantDeroyal Industries, Inc.
Decision Date2016-03-25
Product CodeDXT
Advisory CommitteeCV
DecisionUnknown

Device Summary

DeRoyal Angiography Kits is a medical device manufactured by Deroyal Industries, Inc.. It received FDA 510(k) clearance on 2016-03-25 under approval 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. It is manufactured by Deroyal Industries, Inc.. The 510(k) number is K152978.

When was DeRoyal Angiography Kits approved by the FDA?

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

What company makes DeRoyal Angiography Kits?

DeRoyal Angiography Kits is manufactured by Deroyal Industries, Inc..

What is the FDA product code for DeRoyal Angiography Kits?

The FDA product code for DeRoyal Angiography Kits is DXT.

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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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