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FDA 510(k)

UCLA CCM Abutment

K-Number: K192263 · 2020-02-21

Decision Date2020-02-21
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UCLA CCM Abutment is a medical device manufactured by Dio Corporation. It received FDA 510(k) clearance on 2020-02-21 under approval number K192263. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UCLA CCM Abutment?

UCLA CCM Abutment is a medical device that received FDA 510(k) clearance on 2020-02-21. It is manufactured by Dio Corporation. The 510(k) number is K192263.

When was UCLA CCM Abutment approved by the FDA?

UCLA CCM Abutment received FDA 510(k) clearance on 2020-02-21, under approval number K192263.

What company makes UCLA CCM Abutment?

UCLA CCM Abutment is manufactured by Dio Corporation.

What is the FDA product code for UCLA CCM Abutment?

The FDA product code for UCLA CCM Abutment is NHA.

Other Devices by Dio Corporation

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Related Devices (Code: NHA)

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.