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

TERUMO SYRINGE WITH/WITHOUT NEEDLE

K Number: K083514 · Decision May 22, 2009
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
28
Review Days
177

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Basic Information

Device Name
TERUMO SYRINGE WITH/WITHOUT NEEDLE
K Number
K083514
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terumo Europe N.V.
Date Received
November 26, 2008
Decision Date
May 22, 2009
Product Code
FMF
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
FMF Syringe, Piston

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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)
K230951 Terumo Injection Filter Needle (NF-3013RBKE05M)
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)
Search all 28 clearances from Terumo Europe N.V. →