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FDA 510(k) Applications Submitted by LXN CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990942
03/22/1999
DUET II GLUCOSE CONTROL MONITORING SYSTEM
LXN CORP.
K991754
05/24/1999
GO GLUCOSE MONITORING SYSTEM
LXN CORP.
K002688
08/29/2000
PERSONAL GLUCOSE CONTROL CHARTING SYSTEM
LXN CORP.
K960034
01/03/1996
LXN BLOOD GLUCOSE TEST SYSTEM
LXN CORP.
K962597
07/02/1996
LXN FRUCTOSAMINE TEST SYSTEM
LXN CORP.
K973140
08/21/1997
DUET GLUCOSE CONTROL MONITORING SYSTEM
LXN CORP.
K955629
12/11/1995
LXN FRUCTOSAMINE TEST
LXN CORP.
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