510(k) K060120

TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM by Teco Diagnostics — Product Code CDQ

K060120 is an FDA 510(k) premarket notification submitted by Teco Diagnostics for the device "TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM". The FDA issued a decision of Substantially Equivalent on March 27, 2006. The device falls under product code CDQ (Urease And Glutamic Dehydrogenase, Urea Nitrogen), a Class II device regulated under 21 CFR 862.1770. Teco Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 27, 2006
Date Received
January 17, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Urease And Glutamic Dehydrogenase, Urea Nitrogen
Device Class
Class II
Regulation Number
862.1770
Review Panel
CH
Submission Type