In-Line Diagnostics Corp.
United StatesFDA applicant, unverified
- Devices
- 8
What In-Line Diagnostics Corp. makes
In-Line Diagnostics Corp. manufactures blood monitoring devices, including the CRIT-LINE MONITOR III (CLM III), CRIT-LINE HEMATOCRIT ALERT, CRIT-SCAN II MONITOR, and CRIT-LINE BLOOD CHAMBER WITH E-BEAM.
The company's devices are listed in the FDA 510(k) registry and are classified as Class II medical devices. In-Line Diagnostics Corp. is based in the US.
Catalogue
Crit-Line Monitor Iii (Clm Iii) Ref K992227
Regimes: 510(k) Registry: 510(k)Crit-Line Hematocrit Alert Ref K950942
Regimes: 510(k) Registry: 510(k)Crit-Scan Ii Monitor Ref K983551
Regimes: 510(k) Registry: 510(k)Crit-Line Monitor (Clmiii) Ref K972470
Regimes: 510(k) Registry: 510(k)Crit-Line Hematocrit Alert (Modification) Ref K953875
Regimes: 510(k) Registry: 510(k)Crit-Line Monitor Iii (Clm Iii) Ref K001763
Regimes: 510(k) Registry: 510(k)Modification Of Crit-Line Monitor Iii (Clm Iii) Ref K982412
Regimes: 510(k) Registry: 510(k)Crit-Line Blood Chamber With E-Beam Ref K935958
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does In-Line Diagnostics Corp. have in the registry?
The registry currently lists 8 devices for In-Line Diagnostics Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list In-Line Diagnostics Corp.'s devices?
Among its 8 most recently registered devices, In-Line Diagnostics Corp. has devices listed in FDA 510(k) (8 devices).
What risk classes do In-Line Diagnostics Corp.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for In-Line Diagnostics Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from In-Line Diagnostics Corp. in the registry?
The most recently registered devices listed for In-Line Diagnostics Corp. include CRIT-LINE MONITOR III (CLM III), CRIT-LINE HEMATOCRIT ALERT, CRIT-SCAN II MONITOR and CRIT-LINE MONITOR (CLMIII).