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

FreeStyle Precision Neo H Blood Glucose Monitoring System

K Number: K153330 · Decision Feb 19, 2016
Classifications
1
FEI Numbers
168
Registration Numbers
169
Same Product Code
507
Applicant Total
37
Review Days
92

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Basic Information

Device Name
FreeStyle Precision Neo H Blood Glucose Monitoring System
K Number
K153330
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Diabetes Care, Inc.
Date Received
November 19, 2015
Decision Date
February 19, 2016
Product Code
NBW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NBW System, Test, Blood Glucose, Over The Counter

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NBW), ordered by most recent decision date.

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Other Clearances by Abbott Diabetes Care, Inc.

K Number Device Name
K233537 FreeStyle Libre 3 Continuous Glucose Monitoring System; FreeStyle Libre 2 Flash Glucose Monitoring System
K223435 FreeStyle Libre 3 Continuous Glucose Monitoring System; FreeStyle Libre 2 Flash Glucose Monitoring System
K222447 FreeStyle Libre 2 Flash Glucose Monitoring System; Freestyle Libre 3 Continuous Glucose Monitoring System
K223537 FreeStyle Libre 2 System, FreeStyle Libre 3 System
K213996 FreeStyle Libre 3 Continuous Glucose Monitoring System
K212132 FreeStyle Libre 3 Continuous Glucose Monitoring System
K210943 FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App)
K211102 FreeStyle Libre 2 Flash Glucose Monitoring System
K201761 FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App)
K193371 FreeStyle Libre 2 Flash Glucose Monitoring System
Search all 37 clearances from Abbott Diabetes Care, Inc. →