FDA 510(k)

RadiForce MX317W-PA

K-Number: K242545 · 2025-05-23

Decision Date2025-05-23

Product CodePZZ

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

RadiForce MX317W-PA is the device name listed in this FDA 510(k) record. The listed applicant is Eizo Corporation. It received FDA 510(k) clearance on 2025-05-23 under 510(k) number K242545. The device is classified under product code PZZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RadiForce MX317W-PA?

RadiForce MX317W-PA is a medical device that received FDA 510(k) clearance on 2025-05-23. The listed applicant is Eizo Corporation. The 510(k) number is K242545.

When did RadiForce MX317W-PA receive FDA 510(k) clearance?

RadiForce MX317W-PA received FDA 510(k) clearance on 2025-05-23, under 510(k) number K242545.

Who is the listed applicant for RadiForce MX317W-PA?

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 MX317W-PA?

The FDA product code for RadiForce MX317W-PA is PZZ.

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.

K252030RadiForce GX570; RadiForce GX570-AR K243221RadiForce RX570; RadiForce RX570-AR K241441RadiForce RX670; RadiForce RX670-AR K233465RadiForce MX317W K231066CuratOR EX3242-FD K230684RadiForce MX217

View all 21 devices →

Related Devices (Code: PZZ)

K2331198MP Color LCD Displays C811W, C811WT, PA27 and PA27TShenzhen Beacon Display Technology Co., Ltd.K172922MMPC-4127F1Barco N.V.

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.