FDA 510(k)

ScanNav 신경학 주변 신경 블록

K-번호: K232787 · 2023-10-06

결정일2023-10-06

제품 코드QRG

자문 위원회안내: 의료기기 규제 문서 번역 요청입니다. 회사명, 제품명, FDA, 510(k), PMA, NCT, PMID, 식별자 및 URL을 보존하여 번역하여 주세요. 정책: 의료규제-v1. [원문] AN [번역] 안내

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기기 요약

ScanNav Anatomy Peripheral Nerve Block is the device name listed in this FDA 510(k) record. The listed applicant is Intelligent Ultrasound Limited. It received FDA 510(k) clearance on 2023-10-06 under 510(k) number K232787. The device is classified under product code QRG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the ScanNav Anatomy Peripheral Nerve Block?

ScanNav Anatomy Peripheral Nerve Block is a medical device that received FDA 510(k) clearance on 2023-10-06. The listed applicant is Intelligent Ultrasound Limited. The 510(k) number is K232787.

When did ScanNav Anatomy Peripheral Nerve Block receive FDA 510(k) clearance?

ScanNav Anatomy Peripheral Nerve Block received FDA 510(k) clearance on 2023-10-06, under 510(k) number K232787.

Who is the listed applicant for ScanNav Anatomy Peripheral Nerve Block?

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

What is the FDA product code for ScanNav Anatomy Peripheral Nerve Block?

The FDA product code for ScanNav Anatomy Peripheral Nerve Block is QRG.

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ScanNav 신경학 주변 신경 블록

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: QRG)

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