510(k) K801642

FIAX TEST KIT FOR THEOPHYLLINE QUANT. by Intl. Diagnostic Technology — Product Code KLS

K801642 is an FDA 510(k) premarket notification submitted by Intl. Diagnostic Technology for the device "FIAX TEST KIT FOR THEOPHYLLINE QUANT.". The FDA issued a decision of Substantially Equivalent on August 27, 1980. The device falls under product code KLS (Enzyme Immunoassay, Theophylline), a Class II device regulated under 21 CFR 862.3880. Intl. Diagnostic Technology has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 27, 1980
Date Received
July 17, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Theophylline
Device Class
Class II
Regulation Number
862.3880
Review Panel
TX
Submission Type