FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

ACR LAB Urine Analysis Test System

K Number: K182384 · Decision Jul 26, 2019
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
48
Applicant Total
4
Review Days
329

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Basic Information

Device Name
ACR LAB Urine Analysis Test System
K Number
K182384
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1225
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Healthy.Io, Ltd.
Date Received
August 31, 2018
Decision Date
July 26, 2019
Product Code
JFY
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
JFY Enzymatic Method, Creatinine

Similar 510(k) Clearances

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

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Other Clearances by Healthy.Io, Ltd.

K Number Device Name
K222921 Minuteful-kidney test
K210069 Minuteful - kidney test
K173327 DIP/U.S. Urine Analysis Test System