UCLA CCM Abutment
K-Number: K192263 · 2020-02-21
Device Summary
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. The listed applicant is Dio Corporation. The 510(k) number is K192263.
When did UCLA CCM Abutment receive FDA 510(k) clearance?
UCLA CCM Abutment received FDA 510(k) clearance on 2020-02-21, under 510(k) number K192263.
Who is the listed applicant for UCLA CCM Abutment?
The FDA 510(k) record lists Dio Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UCLA CCM Abutment?
The FDA product code for UCLA CCM Abutment is NHA.
Other records listing Dio Corporation 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.
Related Devices (Code: NHA)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.