FDA 510(k)

CONTOUR® NEXT ONE Blood Glucose Monitoring System

K-번호: K210687 · 2021-08-11

결정일2021-08-11

제품 코드NBW

자문 위원회CH

결정Substantially Equivalent

기기 요약

CONTOUR® NEXT ONE Blood Glucose Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Ascensia Diabetes Care. It received FDA 510(k) clearance on 2021-08-11 under 510(k) number K210687. The device is classified under product code NBW. It was reviewed by the CH advisory panel. Product code NBW falls under the category of OB/GYN, which includes obstetric and gynecological diagnostic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the CONTOUR® NEXT ONE Blood Glucose Monitoring System?

CONTOUR® NEXT ONE Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2021-08-11. The listed applicant is Ascensia Diabetes Care. The 510(k) number is K210687.

When did CONTOUR® NEXT ONE Blood Glucose Monitoring System receive FDA 510(k) clearance?

CONTOUR® NEXT ONE Blood Glucose Monitoring System received FDA 510(k) clearance on 2021-08-11, under 510(k) number K210687.

Who is the listed applicant for CONTOUR® NEXT ONE Blood Glucose Monitoring System?

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

What is the FDA product code for CONTOUR® NEXT ONE Blood Glucose Monitoring System?

The FDA product code for CONTOUR® NEXT ONE Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.

Ascensia Diabetes Care를 신청인으로 등재한 기타 기록

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