In-Line Diagnostics Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K001763 | CRIT-LINE MONITOR III (CLM III) | December 20, 2000 |
| K992227 | CRIT-LINE MONITOR III (CLM III) | July 30, 1999 |
| K983551 | CRIT-SCAN II MONITOR | May 27, 1999 |
| K982412 | MODIFICATION OF CRIT-LINE MONITOR III (CLM III) | October 9, 1998 |
| K972470 | CRIT-LINE MONITOR (CLMIII) | December 11, 1997 |
| K953875 | CRIT-LINE HEMATOCRIT ALERT (MODIFICATION) | July 23, 1996 |
| K950942 | CRIT-LINE HEMATOCRIT ALERT | March 14, 1995 |
| K935958 | CRIT-LINE BLOOD CHAMBER WITH E-BEAM | January 19, 1995 |