NIPRO SAFETOUCH SAFETY FISTULA NEEDLE— 510(k) K002813
Substantially EquivalentNipro Medical Corp.
FDA 510(k) clearance K002813 for NIPRO SAFETOUCH SAFETY FISTULA NEEDLE, Substantially Equivalent on 2000-11-21. Applicant: Nipro Medical Corp..
Clearance details
- Applicant
- Nipro Medical Corp.
- Product code
- Code FIE
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Weston, FL, US
Adverse events under product code FIE
product code FIE- Death
- 2
- Total
- 2
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.