RIGHTEST Blood Glucose Monitoring System Max Tel— 510(k) K231192
Substantially EquivalentBionime Corporation
FDA 510(k) clearance K231192 for RIGHTEST Blood Glucose Monitoring System Max Tel, Substantially Equivalent on 2024-01-19. Applicant: Bionime Corporation. Device class: 2.
Clearance details
- Applicant
- Bionime Corporation
- Product code
- Product code NBW
- Device class
- Class 2
- Regulation
- 21 CFR 862.1345
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Taichung City, TW
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More clearances from Bionime Corporation
view all- K240637 — RIGHTEST Blood Glucose Monitoring System Max Tel
- K221062 — RIGHTEST Lancing Device GD500, GE Lancing Device, iGlucose Lancing Device
- K190564 — Rightest Blood Glucose Monitoring System GM700S, Rightest Blood Glucose Monitoring System GM700SB
- K173638 — Rightest Blood Glucose Monitoring System Max, Rightest Blood Glucose Monitoring System Max Plus, GE Blood Glucose Monitoring System Max, GE Blood Glucose Monitoring System Max Plus
- K173139 — Rightest Blood Glucose Monitoring System Wiz, Rightest Blood Glucose Monitoring System Wiz Plus
Adverse events under product code NBW
product code NBW- Death
- 18
- Injury
- 4,740
- Malfunction
- 42,679
- Other
- 6
- Total
- 47,443
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.