510(k) K980153

DRUG CHECK by Texas Immunology, Inc. — Product Code DIO

K980153 is an FDA 510(k) premarket notification submitted by Texas Immunology, Inc. for the device "DRUG CHECK". The FDA issued a decision of Substantially Equivalent on March 27, 1998. The device falls under product code DIO (Enzyme Immunoassay, Cocaine And Cocaine Metabolites), a Class II device regulated under 21 CFR 862.3250. Texas Immunology, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 27, 1998
Date Received
January 16, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Cocaine And Cocaine Metabolites
Device Class
Class II
Regulation Number
862.3250
Review Panel
TX
Submission Type