FDA 510(k)

Quicktome Software Suite

K-번호: K261795 · 2026-09-10

결정일2026-09-10

제품 코드QIH

자문 위원회RA

결정Substantially Equivalent

기기 요약

Quicktome Software Suite is the device name listed in this FDA 510(k) record. The listed applicant is Omniscient Neurotechnology Pty, Ltd.. It received FDA 510(k) clearance on 2026-09-10 under 510(k) number K261795. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Quicktome Software Suite?

Quicktome Software Suite is a medical device that received FDA 510(k) clearance on 2026-09-10. The listed applicant is Omniscient Neurotechnology Pty, Ltd.. The 510(k) number is K261795.

When did Quicktome Software Suite receive FDA 510(k) clearance?

Quicktome Software Suite received FDA 510(k) clearance on 2026-09-10, under 510(k) number K261795.

Quicktome 소프트웨어 슈트의 등록된 신청자는 누구인가요?

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

What is the FDA product code for Quicktome Software Suite?

The FDA product code for Quicktome Software Suite is QIH.

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FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.

Quicktome Software Suite

기기 요약

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관련 임상시험

관련 기기 (코드: QIH)

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