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.. Device class: 2.
Clearance details
- Applicant
- Terumo Europe N.V.
- Product code
- Code QYM
- Device class
- Class 2
- Regulation
- 21 CFR 880.5570
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Leuven, BE
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