510(k) K800032

FIAX TEST KIT FOR GENTAMICIN QUAN. by Intl. Diagnostic Technology — Product Code LCQ

K800032 is an FDA 510(k) premarket notification submitted by Intl. Diagnostic Technology for the device "FIAX TEST KIT FOR GENTAMICIN QUAN.". The FDA issued a decision of Substantially Equivalent on January 23, 1980. The device falls under product code LCQ (Fluorescent Immunoassay Gentamicin), a Class II device regulated under 21 CFR 862.3450. Intl. Diagnostic Technology has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 23, 1980
Date Received
January 7, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Fluorescent Immunoassay Gentamicin
Device Class
Class II
Regulation Number
862.3450
Review Panel
TX
Submission Type