FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NovoFine 32G Tip (0.23/0.25) x 6 mm ETW (extra thin wall)

K Number: K173479 · Decision Jan 17, 2018
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
14
Review Days
65

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Basic Information

Device Name
NovoFine 32G Tip (0.23/0.25) x 6 mm ETW (extra thin wall)
K Number
K173479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Novo Nordisk, Inc.
Date Received
November 13, 2017
Decision Date
January 17, 2018
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 Novo Nordisk, Inc.

K Number Device Name
K231255 NovoFine® Plus
K210258 NovoFine
K202005 NovoFine Plus 32G Tip x 4 mm
K182387 NovoPen Echo Dial-A-Dose Insulin Delivery Device (Pen Injector)
K162602 NovoPen Echo
K150874 NovoPen Echo Dial-A-Dose Insulin Delivery Device (Pen Injector)
K133738 NOVOFINE PLUS 32G 4 MM
K123766 NOVOPEN ECHO, A DIAL A DOSE INSULIN DELIVERY PEN
K093109 NOVOTWIST NEEDLE, MODELS 30G * 8MM (1/3) 32 G TIP * 5 MM(1/5')
K090111 FLEXPEN NEEDLE
Search all 14 clearances from Novo Nordisk, Inc. →