510(k) K011963

ADVIA 1650 GLUCOSE HEXOKINASE 11 ASSAY by Bayer Corp. — Product Code CFR

K011963 is an FDA 510(k) premarket notification submitted by Bayer Corp. for the device "ADVIA 1650 GLUCOSE HEXOKINASE 11 ASSAY". The FDA issued a decision of Substantially Equivalent on November 20, 2001. The device falls under product code CFR (Hexokinase, Glucose), a Class II device regulated under 21 CFR 862.1345. Bayer Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 20, 2001
Date Received
June 22, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hexokinase, Glucose
Device Class
Class II
Regulation Number
862.1345
Review Panel
CH
Submission Type