FDA 510(k)

ARX 바이러스 이송 미디어 수집 및 이송 시스템

K-번호: K231843 · 2024-03-19

결정일2024-03-19

제품 코드JSM

자문 위원회미 (Original text: MI)

결정대체적으로 동일

기기 요약

ARX Viral Transport Media Collection and Transport System is the device name listed in this FDA 510(k) record. The listed applicant is Arx Sciences, Inc.. It received FDA 510(k) clearance on 2024-03-19 under 510(k) number K231843. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the ARX Viral Transport Media Collection and Transport System?

ARX Viral Transport Media Collection and Transport System is a medical device that received FDA 510(k) clearance on 2024-03-19. The listed applicant is Arx Sciences, Inc.. The 510(k) number is K231843.

When did ARX Viral Transport Media Collection and Transport System receive FDA 510(k) clearance?

ARX Viral Transport Media Collection and Transport System received FDA 510(k) clearance on 2024-03-19, under 510(k) number K231843.

Who is the listed applicant for ARX Viral Transport Media Collection and Transport System?

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

What is the FDA product code for ARX Viral Transport Media Collection and Transport System?

The FDA product code for ARX Viral Transport Media Collection and Transport System is JSM.

Arx Sciences, Inc.를 신청인으로 등재한 기타 기록

K222613ARX Liquid Amies 수집 및 운송 시스템

공식 출처

FDA 데이터베이스에서 보기 →

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