510(k) K954569

IMMULITE THEOPHYLLINE by Diagnostic Products Corp. — Product Code KLS

K954569 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE THEOPHYLLINE". The FDA issued a decision of Substantially Equivalent on November 13, 1995. The device falls under product code KLS (Enzyme Immunoassay, Theophylline), a Class II device regulated under 21 CFR 862.3880. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 13, 1995
Date Received
October 2, 1995
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