FDA 510(k)

Wrist Electronic Sphygmomanometer

K-번호: K193386 · 2021-01-27

신청자Shenzhen Changkun Technology Co., Ltd.

결정일2021-01-27

제품 코드DXN

자문 위원회의료장비 규제 텍스트 번역 [회사명]의 [제품명]은 미국 식약국(FDA)에 등록된 의료장비로, 510(k) 신청을 통해 승인받았습니다. PMA(Premarket Approval) 신청이 진행 중이며, 연구 등록 번호(NCT)는 [NCT 번호]입니다. 논문 등록 번호(PMID)는 [PMID 번호]입니다. 더 자세한 정보는 다음 URL을 참조하세요: [URL] 정책: medical-regulatory-v1

결정Substantially Equivalent

기기 요약

Wrist Electronic Sphygmomanometer is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Changkun Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-01-27 under 510(k) number K193386. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Wrist Electronic Sphygmomanometer?

Wrist Electronic Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2021-01-27. The listed applicant is Shenzhen Changkun Technology Co., Ltd.. The 510(k) number is K193386.

When did Wrist Electronic Sphygmomanometer receive FDA 510(k) clearance?

Wrist Electronic Sphygmomanometer received FDA 510(k) clearance on 2021-01-27, under 510(k) number K193386.

Who is the listed applicant for Wrist Electronic Sphygmomanometer?

The FDA 510(k) record lists Shenzhen Changkun Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Wrist Electronic Sphygmomanometer?

The FDA product code for Wrist Electronic Sphygmomanometer is DXN.

Shenzhen Changkun Technology Co., Ltd.를 신청인으로 등재한 기타 기록

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