510(k) K051526

URITEK-720+ URINE ANALYZER by Teco Diagnostics — Product Code KQO

K051526 is an FDA 510(k) premarket notification submitted by Teco Diagnostics for the device "URITEK-720+ URINE ANALYZER". The FDA issued a decision of Substantially Equivalent on August 16, 2005. The device falls under product code KQO (Automated Urinalysis System), a Class I device regulated under 21 CFR 862.2900. Teco Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 2005
Date Received
June 8, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Automated Urinalysis System
Device Class
Class I
Regulation Number
862.2900
Review Panel
CH
Submission Type