FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Insulin Pen Needle

K Number: K153706 · Decision Aug 29, 2016
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
9
Review Days
250

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Basic Information

Device Name
Insulin Pen Needle
K Number
K153706
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SteriLance Medical (Suzhou), Inc.
Date Received
December 23, 2015
Decision Date
August 29, 2016
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

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Other Clearances by SteriLance Medical (Suzhou), Inc.

K Number Device Name
K261634 Disposable Blood Lancet (Soft)
K244036 Heel Incision Safety Lancet (SteriHeel 2)
K244031 Disposable Blood Lancet (Soft Pro); Disposable Blood Lancet (Softsure); Disposable Blood Lancet (Softsure Pro); Disposable Blood Lancet (Softsense)
K233796 Disposable safety lancet (Impress); Disposable safety lancet (Impress Pro); Disposable safety lancet (Lite4); Disposable blood lancet (Elite); Disposable blood lancet (Elite Pro)
K221521 Disposable Safety Lancet
K221507 Disposable Blood Lancet
K221970 Lancing device
K210745 Heel Incision Safety Lancet