FDA 510(k)

Kurin Blood Culture Collection Set with Kurin Lock Technology

K-번호: K220677 · 2023-04-28

결정일2023-04-28

제품 코드JKA

자문 위원회CH [기업명]의 [제품명]은 미국 식품의약국(FDA)에서 510(k) 등록을 완료한 의료기기입니다. 이 제품은 [PMA] 및 [NCT] 등록을 완료하였으며, [PMID]로 확인할 수 있습니다. 더 자세한 정보는 다음 URL을 참조하세요: [URL].

결정Substantially Equivalent

기기 요약

Kurin Blood Culture Collection Set with Kurin Lock Technology is the device name listed in this FDA 510(k) record. The listed applicant is Kurin, Inc.. It received FDA 510(k) clearance on 2023-04-28 under 510(k) number K220677. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Kurin Blood Culture Collection Set with Kurin Lock Technology?

Kurin Blood Culture Collection Set with Kurin Lock Technology is a medical device that received FDA 510(k) clearance on 2023-04-28. The listed applicant is Kurin, Inc.. The 510(k) number is K220677.

When did Kurin Blood Culture Collection Set with Kurin Lock Technology receive FDA 510(k) clearance?

Kurin Blood Culture Collection Set with Kurin Lock Technology received FDA 510(k) clearance on 2023-04-28, under 510(k) number K220677.

Who is the listed applicant for Kurin Blood Culture Collection Set with Kurin Lock Technology?

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

What is the FDA product code for Kurin Blood Culture Collection Set with Kurin Lock Technology?

The FDA product code for Kurin Blood Culture Collection Set with Kurin Lock Technology is JKA.

Kurin, Inc.를 신청인으로 등재한 기타 기록

K191832Kurin Blood Culture Collection Set with Kurin Lock Technology, Push-Button Needle (Product models M-21221, M-21223, D-21221, D-21223, T-21221, T-21223)K181895Kurin PIV Blood Collection Set with High Pressure

공식 출처

FDA 데이터베이스에서 보기 →

FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.