ClearanceBrief
Company ยท US

In-Line Diagnostics Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2000. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MQSSystem, Hemodialysis, Access Recirculation Monitoring5
GKFInstrument, Hematocrit, Automated1
JPIDevice, Hematocrit Measuring1
KOCAccessories, Blood Circuit, Hemodialysis1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 20, 2000K001763CRIT-LINE MONITOR III (CLM III)
In-Line Diagnostics Corp.
MQS
Jul 30, 1999K992227CRIT-LINE MONITOR III (CLM III)
In-Line Diagnostics Corp.
MQS
May 27, 1999K983551CRIT-SCAN II MONITOR
In-Line Diagnostics Corp.
GKF
Oct 9, 1998K982412MODIFICATION OF CRIT-LINE MONITOR III (CLM III)
In-Line Diagnostics Corp.
MQS
Dec 11, 1997K972470CRIT-LINE MONITOR (CLMIII)
In-Line Diagnostics Corp.
MQS
Jul 23, 1996K953875CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)
In-Line Diagnostics Corp.
MQS
Mar 14, 1995K950942CRIT-LINE HEMATOCRIT ALERT
In-Line Diagnostics Corp.
JPI
Jan 19, 1995K935958CRIT-LINE BLOOD CHAMBER WITH E-BEAM
In-Line Diagnostics Corp.
KOC

Latest recalls

DateFirm and productCodeLinked 510(k)
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