510(k) K013272

ACS: 180 AND ADVIA CENTAUR THEOPHYLLINE 2 ASSAY by Bayer Corp. — Product Code KLS

K013272 is an FDA 510(k) premarket notification submitted by Bayer Corp. for the device "ACS: 180 AND ADVIA CENTAUR THEOPHYLLINE 2 ASSAY". The FDA issued a decision of Substantially Equivalent on October 25, 2001. The device falls under product code KLS (Enzyme Immunoassay, Theophylline), a Class II device regulated under 21 CFR 862.3880. Bayer Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 25, 2001
Date Received
October 1, 2001
Clearance Type
Special
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