FORA GTel Blood Glucose Monitoring System— 510(k) K173505
Substantially EquivalentForacare, Inc.
FDA 510(k) clearance K173505 for FORA GTel Blood Glucose Monitoring System, Substantially Equivalent on 2018-08-09. Applicant: Foracare, Inc..
Clearance details
- Applicant
- Foracare, Inc.
- Product code
- Code NBW
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Moorpark, CA, US
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.