FDA 510(k) FDA class 2 Substantially Equivalent 🇧🇪 Belgium

Terumo Injection Filter Needle (NF-3013RBKE05M)

K Number: K230951 · Decision Oct 18, 2023
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
1
Applicant Total
28
Review Days
197

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Basic Information

Device Name
Terumo Injection Filter Needle (NF-3013RBKE05M)
K Number
K230951
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terumo Europe N.V.
Date Received
April 4, 2023
Decision Date
October 18, 2023
Product Code
QYM
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QYM Ophthalmic Needle

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QYM), ordered by most recent decision date.

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Other Clearances by Terumo Europe N.V.

K Number Device Name
K251447 K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB)
K243309 27G x 1/2 TW K-Pack Surshield Needle (KN-S2713RBT)
K243581 K-Pack Enhance Needle (KH-2713RBBTC and KH-2913RBBTC)
K212095 SurGuard3 Safety Hypodermic Needle
K192057 K-Pack II Needle - 27G x 1/2” Extra Thin Wall, K-Pack II Needle - 27G x 1/2” Ultra Thin Wall, K-Pack II Needle - 30G x 1/2” Extra Thin Wall, K-Pack II Needle - 30G x 1/2” Ultra Thin Wall
K161606 Syringe with fixed needle - For use only with GONAL-F Multi-Dose 600 I/U mL FSH
K151398 K-Pack II Needle - 29G x 5/16 Thin Wall
K150263 K-Pack II Needle-21G x 2
K133894 SURFLO WINGED INFUSION SET WITH FILTER & NEEDLE PROTECTION (SURSHIELD)
K133867 SURFLO WINGED INFUSION SET WITH NEEDLE PROTECTION (SURSHIELD)
Search all 28 clearances from Terumo Europe N.V. →