FDA 510(k)

Blood Pressure Monitor (TMB-2287-B)

K-번호: K240102 · 2024-04-29

신청자Guangdong Transtek Medical Electronics Co., Ltd.

결정일2024-04-29

제품 코드DXN

자문 위원회CV

결정Substantially Equivalent

기기 요약

Blood Pressure Monitor (TMB-2287-B) is the device name listed in this FDA 510(k) record. The listed applicant is Guangdong Transtek Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2024-04-29 under 510(k) number K240102. 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 Blood Pressure Monitor (TMB-2287-B)?

Blood Pressure Monitor (TMB-2287-B) is a medical device that received FDA 510(k) clearance on 2024-04-29. The listed applicant is Guangdong Transtek Medical Electronics Co., Ltd.. The 510(k) number is K240102.

When did Blood Pressure Monitor (TMB-2287-B) receive FDA 510(k) clearance?

Blood Pressure Monitor (TMB-2287-B) received FDA 510(k) clearance on 2024-04-29, under 510(k) number K240102.

Who is the listed applicant for Blood Pressure Monitor (TMB-2287-B)?

The FDA 510(k) record lists Guangdong Transtek Medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Blood Pressure Monitor (TMB-2287-B)?

The FDA product code for Blood Pressure Monitor (TMB-2287-B) is DXN.

Guangdong Transtek Medical Electronics Co., Ltd.를 신청인으로 등재한 기타 기록

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