OKMETER MATCH BLOOD GLUCOSE MONITORING SYSTEM— 510(k) K090609

Substantially Equivalent

Ok Biotech Co., Ltd.

FDA 510(k) clearance K090609 for OKMETER MATCH BLOOD GLUCOSE MONITORING SYSTEM, Substantially Equivalent on 2010-02-04. Applicant: Ok Biotech Co., Ltd..

Clearance details

Applicant: Ok Biotech Co., Ltd.
Product code: Code NBW
Advisory panel: Clinical Chemistry
Date received: 2009-03-06
Decision date: 2010-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsin-Chu City, TW

Download summary PDF View on FDA.gov ↗

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, 2020-01-01 through 2026-04-23. 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.