AutoDensity
K-Number: K251078 · 2025-11-14
Device Summary
Frequently Asked Questions
What is the AutoDensity?
AutoDensity is a medical device that received FDA 510(k) clearance on 2025-11-14. The listed applicant is Eos Imaging. The 510(k) number is K251078.
When did AutoDensity receive FDA 510(k) clearance?
AutoDensity received FDA 510(k) clearance on 2025-11-14, under 510(k) number K251078.
Who is the listed applicant for AutoDensity?
The FDA 510(k) record lists Eos Imaging as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AutoDensity?
The FDA product code for AutoDensity is QIH.
Other records listing Eos Imaging 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: QIH)
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.