FDA 510(k)

Stat Profile Prime ES Comp Plus Analyzer System

K-번호: K191626 · 2019-08-16

결정일2019-08-16

제품 코드JFP

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

Stat Profile Prime ES Comp Plus Analyzer System is the device name listed in this FDA 510(k) record. The listed applicant is Nova Biomedical Corporation. It received FDA 510(k) clearance on 2019-08-16 under 510(k) number K191626. The device is classified under product code JFP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Stat Profile Prime ES Comp Plus Analyzer System?

Stat Profile Prime ES Comp Plus Analyzer System is a medical device that received FDA 510(k) clearance on 2019-08-16. The listed applicant is Nova Biomedical Corporation. The 510(k) number is K191626.

When did Stat Profile Prime ES Comp Plus Analyzer System receive FDA 510(k) clearance?

Stat Profile Prime ES Comp Plus Analyzer System received FDA 510(k) clearance on 2019-08-16, under 510(k) number K191626.

Who is the listed applicant for Stat Profile Prime ES Comp Plus Analyzer System?

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

What is the FDA product code for Stat Profile Prime ES Comp Plus Analyzer System?

The FDA product code for Stat Profile Prime ES Comp Plus Analyzer System is JFP.

Nova Biomedical Corporation를 신청인으로 등재한 기타 기록

K251281Nova Max Creat eGFR Monitoring System K252206Nova Allegro UACR Assay, Nova Allegro Analyzer K221326Nova Allegro HbA1c Assay, Nova Allegro Analyzer K221813Nova Allegro UACR Assay, Nova Allegro Analyzer K232075StatStrip Glucose Hospital Meter System K221900Stat Profile Prime Plus Analyzer System

27개 장치 모두 보기 →

공식 출처

FDA 데이터베이스에서 보기 →

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