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

29G AND 30G K-PACK II NEEDLE

K Number: K062608 · Decision Sep 15, 2006
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
28
Review Days
10

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Basic Information

Device Name
29G AND 30G K-PACK II NEEDLE
K Number
K062608
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terumo Europe N.V.
Date Received
September 5, 2006
Decision Date
September 15, 2006
Product Code
FMI
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
FMI Needle, Hypodermic, Single Lumen

Similar 510(k) Clearances

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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. →