FDA 510(k)

NMI DUAL PORT II

K-번호: K151239 · 2016-06-06

결정일2016-06-06

제품 코드LJT

자문 위원회HO

결정Substantially Equivalent

기기 요약

NMI DUAL PORT II is the device name listed in this FDA 510(k) record. The listed applicant is Navilyst Medical, Inc.. It received FDA 510(k) clearance on 2016-06-06 under 510(k) number K151239. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the NMI DUAL PORT II?

NMI DUAL PORT II is a medical device that received FDA 510(k) clearance on 2016-06-06. The listed applicant is Navilyst Medical, Inc.. The 510(k) number is K151239.

When did NMI DUAL PORT II receive FDA 510(k) clearance?

NMI DUAL PORT II received FDA 510(k) clearance on 2016-06-06, under 510(k) number K151239.

Who is the listed applicant for NMI DUAL PORT II?

The FDA 510(k) record lists Navilyst Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NMI DUAL PORT II?

The FDA product code for NMI DUAL PORT II is LJT.

Navilyst Medical, Inc.를 신청인으로 등재한 기타 기록

관련 기록은 이름, 제품 코드 또는 기타 메타데이터를 사용하여 자동으로 매칭됩니다. 매칭은 검증된 임상, 과학, 기업 또는 규제 상의 관계를 입증하지 않으며, 연결된 공식 출처를 검토하시기 바랍니다.

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관련 기기 (코드: LJT)

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