FDA 510(k)

VERIQA RT EPID 3D

K-번호: K252258 · 2026-04-15

신청자Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla

결정일2026-04-15

제품 코드IYE

자문 위원회[원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.]

결정대체적으로 동일

기기 요약

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.

자주 묻는 질문

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.

Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla를 신청인으로 등재한 기타 기록

K232738BeamDose 소프트웨어 (S080053); BEAMSCAN 소프트웨어, 옵션 참조 dosimetry (S080054.002)

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