RadiForce RX270
K-Number: K223768 · 2023-04-20
Device Summary
Frequently Asked Questions
What is the RadiForce RX270?
RadiForce RX270 is a medical device that received FDA 510(k) clearance on 2023-04-20. The listed applicant is Eizo Corporation. The 510(k) number is K223768.
When did RadiForce RX270 receive FDA 510(k) clearance?
RadiForce RX270 received FDA 510(k) clearance on 2023-04-20, under 510(k) number K223768.
Who is the listed applicant for RadiForce RX270?
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 RX270?
The FDA product code for RadiForce RX270 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.