FDA 510(k)

PodSKAN HF 诊断 X線システム

K番号: K231761 · 2023-10-27

決定日2023-10-27

製品コードKPR

諮問委員会RA （注：由于原文中未提供具体的医疗设备监管文本内容，因此无法进行翻译。请提供具体的文本内容以便进行翻译。）

決定大幅同等

医療機器の概要

PodSKAN HF Diagnostic X-ray System is the device name listed in this FDA 510(k) record. The listed applicant is Skanray Technologies Limited. It received FDA 510(k) clearance on 2023-10-27 under 510(k) number K231761. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the PodSKAN HF Diagnostic X-ray System?

PodSKAN HF Diagnostic X-ray System is a medical device that received FDA 510(k) clearance on 2023-10-27. The listed applicant is Skanray Technologies Limited. The 510(k) number is K231761.

When did PodSKAN HF Diagnostic X-ray System receive FDA 510(k) clearance?

PodSKAN HF Diagnostic X-ray System received FDA 510(k) clearance on 2023-10-27, under 510(k) number K231761.

Who is the listed applicant for PodSKAN HF Diagnostic X-ray System?

The FDA 510(k) record lists Skanray Technologies Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PodSKAN HF Diagnostic X-ray System?

The FDA product code for PodSKAN HF Diagnostic X-ray System is KPR.

申請者としてSkanray Technologies Limitedを記載するその他の記録

K251893SKAN C PULSAR K220518SKANRAD 400 K212940Skanmobile、Skanmobile-Dr

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