FDA 510(k)

BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit

K-번호: K180438 · 2018-03-20

신청자Bd

결정일2018-03-20

제품 코드PSZ

자문 위원회MI

결정Substantially Equivalent

기기 요약

BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit is the device name listed in this FDA 510(k) record. The listed applicant is Bd. It received FDA 510(k) clearance on 2018-03-20 under 510(k) number K180438. The device is classified under product code PSZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit?

BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit is a medical device that received FDA 510(k) clearance on 2018-03-20. The listed applicant is Bd. The 510(k) number is K180438.

When did BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit receive FDA 510(k) clearance?

BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit received FDA 510(k) clearance on 2018-03-20, under 510(k) number K180438.

Who is the listed applicant for BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit?

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

What is the FDA product code for BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit?

The FDA product code for BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit is PSZ.

Bd를 신청인으로 등재한 기타 기록

K253445BD Surgiphor™ 1000 mL Antimicrobial Irrigation System (910120)K240257Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit K232434BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit K223016BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived Kit K221504BD Surgiphor™ Antimicrobial Irrigation System

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