FDA 510(k)

IODR1717 / IODR1417 / IODR1417-GF (디지털 평면 X선探测器)

K-번호: K241346 · 2024-11-07

결정일2024-11-07

제품 코드MQB

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

결정대체적으로 동일

기기 요약

IODR1717 / IODR1417 / IODR1417-GF (Digital Flat Panel X-ray Detector) is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Imaging Healthcare, Inc.. It received FDA 510(k) clearance on 2024-11-07 under 510(k) number K241346. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the IODR1717 / IODR1417 / IODR1417-GF (Digital Flat Panel X-ray Detector)?

IODR1717 / IODR1417 / IODR1417-GF (Digital Flat Panel X-ray Detector) is a medical device that received FDA 510(k) clearance on 2024-11-07. The listed applicant is Aspen Imaging Healthcare, Inc.. The 510(k) number is K241346.

When did IODR1717 / IODR1417 / IODR1417-GF (Digital Flat Panel X-ray Detector) receive FDA 510(k) clearance?

IODR1717 / IODR1417 / IODR1417-GF (Digital Flat Panel X-ray Detector) received FDA 510(k) clearance on 2024-11-07, under 510(k) number K241346.

Who is the listed applicant for IODR1717 / IODR1417 / IODR1417-GF (Digital Flat Panel X-ray Detector)?

The FDA 510(k) record lists Aspen Imaging Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IODR1717 / IODR1417 / IODR1417-GF (Digital Flat Panel X-ray Detector)?

The FDA product code for IODR1717 / IODR1417 / IODR1417-GF (Digital Flat Panel X-ray Detector) is MQB.

Aspen Imaging Healthcare, Inc.를 신청인으로 등재한 기타 기록

K241425AspenView

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