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FDA 510(k) Applications Submitted by IN-LINE DIAGNOSTICS CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K953875
06/28/1995
CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)
IN-LINE DIAGNOSTICS CORP.
K001763
06/12/2000
CRIT-LINE MONITOR III (CLM III)
IN-LINE DIAGNOSTICS CORP.
K992227
07/02/1999
CRIT-LINE MONITOR III (CLM III)
IN-LINE DIAGNOSTICS CORP.
K982412
07/13/1998
MODIFICATION OF CRIT-LINE MONITOR III (CLM III)
IN-LINE DIAGNOSTICS CORP.
K983551
10/09/1998
CRIT-SCAN II MONITOR
IN-LINE DIAGNOSTICS CORP.
K972470
07/01/1997
CRIT-LINE MONITOR (CLMIII)
IN-LINE DIAGNOSTICS CORP.
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