510(k) K173327

DIP/U.S. Urine Analysis Test System by Healthy.Io, Ltd. — Product Code JIL

K173327 is an FDA 510(k) premarket notification submitted by Healthy.Io, Ltd. for the device "DIP/U.S. Urine Analysis Test System". The FDA issued a decision of Substantially Equivalent on July 18, 2018. The device falls under product code JIL (Method, Enzymatic, Glucose (Urinary, Non-Quantitative)), a Class II device regulated under 21 CFR 862.1340. Healthy.Io, Ltd. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 18, 2018
Date Received
October 20, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
Device Class
Class II
Regulation Number
862.1340
Review Panel
CH
Submission Type