Preat Abutments
K-Number: K183518 · 2019-03-18
Device Summary
Frequently Asked Questions
What is the Preat Abutments?
Preat Abutments is a medical device that received FDA 510(k) clearance on 2019-03-18. The listed applicant is Preat Corporation. The 510(k) number is K183518.
When did Preat Abutments receive FDA 510(k) clearance?
Preat Abutments received FDA 510(k) clearance on 2019-03-18, under 510(k) number K183518.
Who is the listed applicant for Preat Abutments?
The FDA 510(k) record lists Preat Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Preat Abutments?
The FDA product code for Preat Abutments is NHA.
Other records listing Preat 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.