FDA 510(k)

3mensio Workstation

K番号: K153736 · 2016-05-27

決定日2016-05-27

製品コードLLZ

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

3mensio Workstation is the device name listed in this FDA 510(k) record. The listed applicant is Pie Medical Imaging BV. It received FDA 510(k) clearance on 2016-05-27 under 510(k) number K153736. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the 3mensio Workstation?

3mensio Workstation is a medical device that received FDA 510(k) clearance on 2016-05-27. The listed applicant is Pie Medical Imaging BV. The 510(k) number is K153736.

When did 3mensio Workstation receive FDA 510(k) clearance?

3mensio Workstation received FDA 510(k) clearance on 2016-05-27, under 510(k) number K153736.

Who is the listed applicant for 3mensio Workstation?

The FDA 510(k) record lists Pie Medical Imaging BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3mensio Workstation?

The FDA product code for 3mensio Workstation is LLZ.

申請者としてPie Medical Imaging BVを記載するその他の記録

K2503303mensio Workstation K232147CAAS ウークステーション K232007CAAS MRソリューション K212376Caas クアリア K181825CAAS MRソリューション K180019CAAS ウークステーション

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