510(k) K003987

URS-1K (KETONE TESST) by Teco Diagnostics — Product Code JIN

K003987 is an FDA 510(k) premarket notification submitted by Teco Diagnostics for the device "URS-1K (KETONE TESST)". The FDA issued a decision of Substantially Equivalent on April 26, 2001. The device falls under product code JIN (Nitroprusside, Ketones (Urinary, Non-Quant.)), a Class I device regulated under 21 CFR 862.1435. Teco Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 26, 2001
Date Received
December 26, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nitroprusside, Ketones (Urinary, Non-Quant.)
Device Class
Class I
Regulation Number
862.1435
Review Panel
CH
Submission Type