SUPER-FINE PEN NEEDLE— 510(k) K092016
Substantially EquivalentStat Medical Devices, Inc.
FDA 510(k) clearance K092016 for SUPER-FINE PEN NEEDLE, Substantially Equivalent on 2009-10-02. Applicant: Stat Medical Devices, Inc..
Clearance details
- Applicant
- Stat Medical Devices, Inc.
- Product code
- Code FMI
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- North Miami Beach, FL, US
Adverse events under product code FMI
product code FMI- Death
- 28
- Injury
- 1,517
- Malfunction
- 23,981
- Other
- 18
- Total
- 25,544
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.