510(k) K131441
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