510(k) K131441

LIAISON TOXO IGM II, LIAISON CONTROL TOXO IGM II by DiaSorin, Inc. — Product Code LGD

K131441 is an FDA 510(k) premarket notification submitted by DiaSorin, Inc. for the device "LIAISON TOXO IGM II, LIAISON CONTROL TOXO IGM II". The FDA issued a decision of Substantially Equivalent on August 9, 2013. The device falls under product code LGD (Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii), a Class II device regulated under 21 CFR 866.3780. DiaSorin, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 9, 2013
Date Received
May 20, 2013
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii
Device Class
Class II
Regulation Number
866.3780
Review Panel
MI
Submission Type