FDA 510(k)

iSR'obot MRI-US 합성

K-번호: K161109 · 2016-10-06

결정일2016-10-06

제품 코드LLZ

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

결정대체적으로 동일

기기 요약

iSR'obot MRI-US Fusion is the device name listed in this FDA 510(k) record. The listed applicant is Biobot Surgical Pte., Ltd.. It received FDA 510(k) clearance on 2016-10-06 under 510(k) number K161109. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the iSR'obot MRI-US Fusion?

iSR'obot MRI-US Fusion is a medical device that received FDA 510(k) clearance on 2016-10-06. The listed applicant is Biobot Surgical Pte., Ltd.. The 510(k) number is K161109.

When did iSR'obot MRI-US Fusion receive FDA 510(k) clearance?

iSR'obot MRI-US Fusion received FDA 510(k) clearance on 2016-10-06, under 510(k) number K161109.

Who is the listed applicant for iSR'obot MRI-US Fusion?

The FDA 510(k) record lists Biobot Surgical Pte., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for iSR'obot MRI-US Fusion?

The FDA product code for iSR'obot MRI-US Fusion is LLZ.

Biobot Surgical Pte., Ltd.를 신청인으로 등재한 기타 기록

K232320iSR`로봇 모나리자 2.0 K213411iSR’obot 모나리자 2.0 K203659iSR'obot 몬라리자 1.0 K163502iSR'obot 생검 키트

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