510(k) K890154

MODIFIED LABYSYSTEMS' TOXOPLASMA GONDII IGG EIA by Labsystems, Inc. — Product Code LGD

K890154 is an FDA 510(k) premarket notification submitted by Labsystems, Inc. for the device "MODIFIED LABYSYSTEMS' TOXOPLASMA GONDII IGG EIA". The FDA issued a decision of Substantially Equivalent on February 7, 1989. The device falls under product code LGD (Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii), a Class II device regulated under 21 CFR 866.3780. Labsystems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 7, 1989
Date Received
January 12, 1989
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