FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Sure-Fine Insulin Syringes

K Number: K152879 · Decision Sep 9, 2016
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
7
Review Days
345

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Basic Information

Device Name
Sure-Fine Insulin Syringes
K Number
K152879
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shina Med Corporation
Date Received
September 30, 2015
Decision Date
September 9, 2016
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 Shina Med Corporation

K Number Device Name
K250510 Sure-Fine Insulin Syringes
K250658 SureFine Pen Needle
K231165 Shina Syringe; Shina Safety Syringe
K210848 Sure-Fine Insulin Syringes
K191531 Sure-Fine Insulin Syringes
K152877 SureFine Pen Needle