FDA 510(k)

퀴버 흡수 펌프

K-번호: K232831 · 2024-02-22

결정일2024-02-22

제품 코드BTA

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

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기기 요약

Quiver Aspiration Pump is the device name listed in this FDA 510(k) record. The listed applicant is Anoxia Medical, Inc.. It received FDA 510(k) clearance on 2024-02-22 under 510(k) number K232831. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Quiver Aspiration Pump?

Quiver Aspiration Pump is a medical device that received FDA 510(k) clearance on 2024-02-22. The listed applicant is Anoxia Medical, Inc.. The 510(k) number is K232831.

When did Quiver Aspiration Pump receive FDA 510(k) clearance?

Quiver Aspiration Pump received FDA 510(k) clearance on 2024-02-22, under 510(k) number K232831.

Who is the listed applicant for Quiver Aspiration Pump?

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

What is the FDA product code for Quiver Aspiration Pump?

The FDA product code for Quiver Aspiration Pump is BTA.

Anoxia Medical, Inc.를 신청인으로 등재한 기타 기록

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