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FDA 510(k)

VERIQA RT EPID 3D

K-Number: K252258 · 2026-04-15

Decision Date2026-04-15
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VERIQA RT EPID 3D is a medical device manufactured by Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla. It received FDA 510(k) clearance on 2026-04-15 under approval number K252258. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIQA RT EPID 3D?

VERIQA RT EPID 3D is a medical device that received FDA 510(k) clearance on 2026-04-15. It is manufactured by Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla. The 510(k) number is K252258.

When was VERIQA RT EPID 3D approved by the FDA?

VERIQA RT EPID 3D received FDA 510(k) clearance on 2026-04-15, under approval number K252258.

What company makes VERIQA RT EPID 3D?

VERIQA RT EPID 3D is manufactured by Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla.

What is the FDA product code for VERIQA RT EPID 3D?

The FDA product code for VERIQA RT EPID 3D is IYE.

Other Devices by Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla

Related Devices (Code: IYE)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.