Terumo Injection Filter Needle (NF-3013RBKE05M)— 510(k) K230951
Substantially EquivalentTerumo Europe N.V.
FDA 510(k) clearance K230951 for Terumo Injection Filter Needle (NF-3013RBKE05M), Substantially Equivalent on 2023-10-18. Applicant: Terumo Europe N.V..
Clearance details
- Applicant
- Terumo Europe N.V.
- Product code
- Code QYM
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Leuven, BE
Data sourced from openFDA. This site is unofficial and independent of the FDA.