510(k) K961462

CEDIA THEOPHYLLINE ASSAY by Boehringer Mannheim Corp. — Product Code KLS

K961462 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "CEDIA THEOPHYLLINE ASSAY". The FDA issued a decision of Substantially Equivalent on June 27, 1996. The device falls under product code KLS (Enzyme Immunoassay, Theophylline), a Class II device regulated under 21 CFR 862.3880. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 27, 1996
Date Received
April 17, 1996
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