FDA 510(k)

Annalise Enterprise CTB Triage-OH

K-번호: K231094 · 2023-08-15

결정일2023-08-15

제품 코드QAS

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

결정대체적으로 동일

기기 요약

Annalise Enterprise CTB Triage-OH is the device name listed in this FDA 510(k) record. The listed applicant is Annalise-Ai Pty , Ltd.. It received FDA 510(k) clearance on 2023-08-15 under 510(k) number K231094. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Annalise Enterprise CTB Triage-OH?

Annalise Enterprise CTB Triage-OH is a medical device that received FDA 510(k) clearance on 2023-08-15. The listed applicant is Annalise-Ai Pty , Ltd.. The 510(k) number is K231094.

When did Annalise Enterprise CTB Triage-OH receive FDA 510(k) clearance?

Annalise Enterprise CTB Triage-OH received FDA 510(k) clearance on 2023-08-15, under 510(k) number K231094.

Who is the listed applicant for Annalise Enterprise CTB Triage-OH?

The FDA 510(k) record lists Annalise-Ai Pty , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Annalise Enterprise CTB Triage-OH?

The FDA product code for Annalise Enterprise CTB Triage-OH is QAS.

Annalise-Ai Pty , Ltd.를 신청인으로 등재한 기타 기록

K231767Annalise Enterprise CTB Triage Trauma K231384Annalise Enterprise CTB Triage Trauma K223240Annalise Enterprise CTB Triage Trauma K222179Annalise Enterprise CXR Triage Trauma K222268Annalise Enterprise CXR Triage Trauma

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