FDA 510(k)

Artiglass NRFitTM Tip L.O.R. 유리注射기

K-번호: K213800 · 2022-05-19

결정일2022-05-19

제품 코드QEH

자문 위원회HO

결정Substantially Equivalent

기기 요약

Artiglass NRFitTM Tip L.O.R. Glass Syringes is the device name listed in this FDA 510(k) record. The listed applicant is Artiglass Srl. It received FDA 510(k) clearance on 2022-05-19 under 510(k) number K213800. The device is classified under product code QEH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Artiglass NRFitTM Tip L.O.R. Glass Syringes?

Artiglass NRFitTM Tip L.O.R. Glass Syringes is a medical device that received FDA 510(k) clearance on 2022-05-19. The listed applicant is Artiglass Srl. The 510(k) number is K213800.

When did Artiglass NRFitTM Tip L.O.R. Glass Syringes receive FDA 510(k) clearance?

Artiglass NRFitTM Tip L.O.R. Glass Syringes received FDA 510(k) clearance on 2022-05-19, under 510(k) number K213800.

Who is the listed applicant for Artiglass NRFitTM Tip L.O.R. Glass Syringes?

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

What is the FDA product code for Artiglass NRFitTM Tip L.O.R. Glass Syringes?

The FDA product code for Artiglass NRFitTM Tip L.O.R. Glass Syringes is QEH.

공식 출처

FDA 데이터베이스에서 보기 →

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

Artiglass NRFitTM Tip L.O.R. 유리注射기

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: QEH)

공식 출처