FDA 510(k)

Acare Suction Unit

K-번호: K182950 · 2019-08-23

결정일2019-08-23

제품 코드JCX

자문 위원회SU [원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.]

결정Substantially Equivalent

기기 요약

Acare Suction Unit is the device name listed in this FDA 510(k) record. The listed applicant is Acare Technology Co., Ltd.. It received FDA 510(k) clearance on 2019-08-23 under 510(k) number K182950. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Acare Suction Unit?

Acare Suction Unit is a medical device that received FDA 510(k) clearance on 2019-08-23. The listed applicant is Acare Technology Co., Ltd.. The 510(k) number is K182950.

When did Acare Suction Unit receive FDA 510(k) clearance?

Acare Suction Unit received FDA 510(k) clearance on 2019-08-23, under 510(k) number K182950.

Who is the listed applicant for Acare Suction Unit?

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

What is the FDA product code for Acare Suction Unit?

The FDA product code for Acare Suction Unit is JCX.

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Acare Suction Unit

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: JCX)

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