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

GLP systems Track

K Number: K213486 · Decision Mar 10, 2022
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
160
Applicant Total
25
Review Days
132

Basic Information

Device Name
GLP systems Track
K Number
K213486
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1665
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Laboratories
Date Received
October 29, 2021
Decision Date
March 10, 2022
Product Code
JGS
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
JGS Electrode, Ion Specific, Sodium

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