510(k) K871905

TOXOPLASMA GONDII IGG ELISA by Electro-Nucleonics Laboratories, Inc. — Product Code LGD

K871905 is an FDA 510(k) premarket notification submitted by Electro-Nucleonics Laboratories, Inc. for the device "TOXOPLASMA GONDII IGG ELISA". The FDA issued a decision of Substantially Equivalent on July 30, 1987. The device falls under product code LGD (Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii), a Class II device regulated under 21 CFR 866.3780. Electro-Nucleonics Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 30, 1987
Date Received
May 15, 1987
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