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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