FDA 510(k)

FlowStar Touch Digital Mixer Flowmeter

K-번호: K222794 · 2023-07-28

결정일2023-07-28

제품 코드BZR

자문 위원회안내: 의료기기 규제 문서 번역 요청입니다. 회사명, 제품명, FDA, 510(k), PMA, NCT, PMID, 식별자 및 URL을 보존하여 번역하여 주세요. 정책: 의료규제-v1. [원문] AN [번역] 안내

결정Substantially Equivalent

기기 요약

FlowStar Touch Digital Mixer Flowmeter is the device name listed in this FDA 510(k) record. The listed applicant is Baldus Sedation GmbH & Co. KG. It received FDA 510(k) clearance on 2023-07-28 under 510(k) number K222794. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the FlowStar Touch Digital Mixer Flowmeter?

FlowStar Touch Digital Mixer Flowmeter is a medical device that received FDA 510(k) clearance on 2023-07-28. The listed applicant is Baldus Sedation GmbH & Co. KG. The 510(k) number is K222794.

When did FlowStar Touch Digital Mixer Flowmeter receive FDA 510(k) clearance?

FlowStar Touch Digital Mixer Flowmeter received FDA 510(k) clearance on 2023-07-28, under 510(k) number K222794.

Who is the listed applicant for FlowStar Touch Digital Mixer Flowmeter?

The FDA 510(k) record lists Baldus Sedation GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FlowStar Touch Digital Mixer Flowmeter?

The FDA product code for FlowStar Touch Digital Mixer Flowmeter is BZR.

Baldus Sedation GmbH & Co. KG를 신청인으로 등재한 기타 기록

K230987FlowStar Analog Mixer Flowmeter

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