CONTOUR® PLUS BLUE Blood Glucose Monitoring System; CONTOUR® NEXT GEN Blood Glucose Monitoring System; CONTOUR® NEXT ONE Blood Glucose Monitoring System

FDA 510(k) K260545 · Ascensia Diabetes Care

Substantially Equivalent

510(k) numberK260545

Submission

Device name
CONTOUR® PLUS BLUE Blood Glucose Monitoring System; CONTOUR® NEXT GEN Blood Glucose Monitoring System; CONTOUR® NEXT ONE Blood Glucose Monitoring System
Applicant
Ascensia Diabetes Care
Valhalla, NY, US
Received
February 18, 2026
Decision date
August 27, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NBW – System, Test, Blood Glucose, Over The Counter
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1345
Specialty
Clinical Chemistry

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More from Bionime Corporation

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K231679CONTOUR® PLUS BLUE Blood Glucose Monitoring SystemNBW · Traditional 02/23/2024SE
K193407Contour® next GEN Blood Glucose Monitoring SystemNBW · Traditional 12/23/2021SE
K210687CONTOUR® NEXT ONE Blood Glucose Monitoring SystemNBW · Special 08/11/2021SE
K191286CONTOUR® NEXT Blood Glucose Monitoring System, CONTOUR® NEXT USB Blood Glucose…NBW · Special 11/08/2019SE
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Questions and answers

When was CONTOUR® PLUS BLUE Blood Glucose Monitoring System; CONTOUR® NEXT GEN Blood Glucose Monitoring System; CONTOUR® NEXT ONE Blood Glucose Monitoring System cleared by the FDA?

CONTOUR® PLUS BLUE Blood Glucose Monitoring System; CONTOUR® NEXT GEN Blood Glucose Monitoring System; CONTOUR® NEXT ONE Blood Glucose Monitoring System (K260545) received a 510(k) decision of Substantially Equivalent on August 27, 2026, 190 days after the submission was received.

What is the product code of K260545?

The FDA product code is NBW – System, Test, Blood Glucose, Over The Counter, a Class II (moderate risk) device regulated under 21 CFR 862.1345.