RIGHTEST Blood Glucose Monitoring System Max Tel

FDA 510(k) K240637 · Bionime Corporation

Substantially Equivalent

510(k) numberK240637

Submission

Device name
RIGHTEST Blood Glucose Monitoring System Max Tel
Applicant
Bionime Corporation
Taichung City, TW
Received
March 6, 2024
Decision date
November 4, 2024
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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K231192RIGHTEST Blood Glucose Monitoring System Max TelNBW · Traditional 01/19/2024SE
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K190564Rightest Blood Glucose Monitoring System GM700S, Rightest Blood Glucose Monitoring…NBW · Traditional 06/02/2019SE
K173638Rightest Blood Glucose Monitoring System Max, Rightest Blood Glucose Monitoring System…NBW · Traditional 08/17/2018SE
K173139Rightest Blood Glucose Monitoring System Wiz, Rightest Blood Glucose Monitoring System…NBW · Traditional 06/19/2018SE
K170143GE Blood Glucose Monitoring System 180, GE Blood Glucose Monitoring System 182, Rightest…NBW · Traditional 07/06/2017SE
K161790iGlucose Blood Glucose Monitoring SystemNBW · Traditional 05/02/2017SE
K140210Rightest Blood Glucose Monitoring System ( GM720, Rightest Professional BGMS GM720NBW · Traditional 08/22/2014SE
K133003Rightest Control SolutionJJX · Traditional 10/24/2013SE
K123008Rightest Blood Glucose Monitoring System GM700 GE GE200 Blood Glucose Monitoring System…NBW · Special 01/25/2013SE

Questions and answers

When was RIGHTEST Blood Glucose Monitoring System Max Tel cleared by the FDA?

RIGHTEST Blood Glucose Monitoring System Max Tel (K240637) received a 510(k) decision of Substantially Equivalent on November 4, 2024, 243 days after the submission was received.

What is the product code of K240637?

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.