510(k) K112790

AXIS-SHIELD 3-REAGENT HOMOCYSTEINE ASSAY FOR SYNCHRON by Axis-Shield Diagnostics, Ltd. — Product Code LPS

K112790 is an FDA 510(k) premarket notification submitted by Axis-Shield Diagnostics, Ltd. for the device "AXIS-SHIELD 3-REAGENT HOMOCYSTEINE ASSAY FOR SYNCHRON". The FDA issued a decision of Substantially Equivalent on May 7, 2012. The device falls under product code LPS (Urinary Homocystine (Nonquantitative) Test System), a Class II device regulated under 21 CFR 862.1377. Axis-Shield Diagnostics, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 7, 2012
Date Received
September 26, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Urinary Homocystine (Nonquantitative) Test System
Device Class
Class II
Regulation Number
862.1377
Review Panel
CH
Submission Type