510(k) K875113

TOXOSTAT M TEST KIT by Whittaker Bioproducts, Inc. — Product Code LGD

K875113 is an FDA 510(k) premarket notification submitted by Whittaker Bioproducts, Inc. for the device "TOXOSTAT M TEST KIT". The FDA issued a decision of Substantially Equivalent on April 12, 1988. The device falls under product code LGD (Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii), a Class II device regulated under 21 CFR 866.3780. Whittaker Bioproducts, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 12, 1988
Date Received
December 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