FDA 510(k)

BP Go (BPP-855)

K-번호: K261061 · 2026-08-13

결정일2026-08-13

제품 코드DXN

자문 위원회CV

결정Substantially Equivalent

기기 요약

BP Go (BPP-855) is the device name listed in this FDA 510(k) record. The listed applicant is Wellvii, Inc.. It received FDA 510(k) clearance on 2026-08-13 under 510(k) number K261061. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

BP Go (BPP-855)는 무엇인가요?

BP Go (BPP-855) is a medical device that received FDA 510(k) clearance on 2026-08-13. The listed applicant is Wellvii, Inc.. The 510(k) number is K261061.

When did BP Go (BPP-855) receive FDA 510(k) clearance?

BP Go (BPP-855) received FDA 510(k) clearance on 2026-08-13, under 510(k) number K261061.

Who is the listed applicant for BP Go (BPP-855)?

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

What is the FDA product code for BP Go (BPP-855)?

The FDA product code for BP Go (BPP-855) is DXN.

Wellvii, 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: DXN)

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