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In-Line Diagnostics Corp.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K001763	CRIT-LINE MONITOR III (CLM III)	MQS	2000-12-20	View
510(k)	K992227	CRIT-LINE MONITOR III (CLM III)	MQS	1999-07-30	View
510(k)	K983551	CRIT-SCAN II MONITOR	GKF	1999-05-27	View
510(k)	K982412	MODIFICATION OF CRIT-LINE MONITOR III (CLM III)	MQS	1998-10-09	View
510(k)	K972470	CRIT-LINE MONITOR (CLMIII)	MQS	1997-12-11	View
510(k)	K953875	CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)	MQS	1996-07-23	View
510(k)	K950942	CRIT-LINE HEMATOCRIT ALERT	JPI	1995-03-14	View
510(k)	K935958	CRIT-LINE BLOOD CHAMBER WITH E-BEAM	KOC	1995-01-19	View

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