In-Line Diagnostics Corp.
In-Line Diagnostics Corp. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2000.
Top product codes for In-Line Diagnostics Corp.
Recent clearances by In-Line Diagnostics Corp.
- K001763 — CRIT-LINE MONITOR III (CLM III)
- K992227 — CRIT-LINE MONITOR III (CLM III)
- K983551 — CRIT-SCAN II MONITOR
- K982412 — MODIFICATION OF CRIT-LINE MONITOR III (CLM III)
- K972470 — CRIT-LINE MONITOR (CLMIII)
- K953875 — CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)
- K950942 — CRIT-LINE HEMATOCRIT ALERT
- K935958 — CRIT-LINE BLOOD CHAMBER WITH E-BEAM
Data sourced from openFDA. This site is unofficial and independent of the FDA.