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FDA 510(k)

VERIQA RT EPID 3D

K-Number: K252258 · 2026-04-15

ApplicantPtw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla
Decision Date2026-04-15
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VERIQA RT EPID 3D is the device name listed in this FDA 510(k) record. The listed applicant is Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla. It received FDA 510(k) clearance on 2026-04-15 under 510(k) 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. The listed applicant is Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla. The 510(k) number is K252258.

When did VERIQA RT EPID 3D receive FDA 510(k) clearance?

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

Who is the listed applicant for VERIQA RT EPID 3D?

The FDA 510(k) record lists Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla 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.

K232738BeamDose software (S080053); BEAMSCAN software, option reference dosimetry (S080054.002)

Related Devices (Code: IYE)

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.

K261856Halcyon, Ethos Radiotherapy System (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SAK253004LUNA 3DLap GmbH Laser ApplikationenK260792AerFrame Patient Immobilization System (AFPIS)Stabilix, LLCK253962ClearCheck (RADCC V2.7)Radformation, Inc.K253012AlignRT Plus (8.0)Vision Rt, Ltd.

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.

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