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FDA 510(k)

D2P

K-Number: K183489 · 2019-08-29

Applicant3D Systems, Inc.
Decision Date2019-08-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

D2P is a medical device manufactured by 3D Systems, Inc.. It received FDA 510(k) clearance on 2019-08-29 under approval number K183489. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D2P?

D2P is a medical device that received FDA 510(k) clearance on 2019-08-29. It is manufactured by 3D Systems, Inc.. The 510(k) number is K183489.

When was D2P approved by the FDA?

D2P received FDA 510(k) clearance on 2019-08-29, under approval number K183489.

What company makes D2P?

D2P is manufactured by 3D Systems, Inc..

What is the FDA product code for D2P?

The FDA product code for D2P is LLZ.

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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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