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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