RadiForce MX217
K-Number: K230684 · 2023-05-12
Device Summary
Frequently Asked Questions
What is the RadiForce MX217?
RadiForce MX217 is a medical device that received FDA 510(k) clearance on 2023-05-12. The listed applicant is Eizo Corporation. The 510(k) number is K230684.
When did RadiForce MX217 receive FDA 510(k) clearance?
RadiForce MX217 received FDA 510(k) clearance on 2023-05-12, under 510(k) number K230684.
Who is the listed applicant for RadiForce MX217?
The FDA 510(k) record lists Eizo Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RadiForce MX217?
The FDA product code for RadiForce MX217 is PGY.
Other records listing Eizo 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: PGY)
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.