Litton Datamedix
Country not established
- Devices
- 6
What Litton Datamedix makes
Litton Datamedix manufactures non-invasive blood pressure monitors, ultrasound coupling gels, cardiac monitoring devices (including electrocardiogram recorders and pulse oximeters), and defibrillators. Their portfolio also includes transcutaneous carbon dioxide (CO₂) monitoring systems for patient care.
These devices are regulated under Class II classifications in the US, with some authorised via FDA 510(k) clearances and others through FDA PMA approvals. The company’s products are listed in the FDA’s regulatory databases for medical devices.
Catalogue
Litton Datamedix Blood Pressure Monitor Ni Ref K853599
Regimes: 510(k) Registry: 510(k)Ultrasound Gel Ref K850290
Regimes: 510(k) Registry: 510(k)Servocard Scp-840 Ref K842312
Regimes: 510(k) Registry: 510(k)Servomed Oxymonito Smk 363 Ref K842497
Regimes: 510(k) Registry: 510(k)Servocard Defibrillator Scp-851 Ref K842235
Regimes: 510(k) Registry: 510(k)Litton Transcutaneous CO2 System Ref P850087
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Litton Datamedix have in the registry?
The registry currently lists 6 devices for Litton Datamedix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Litton Datamedix's devices?
Among its 6 most recently registered devices, Litton Datamedix has devices listed in FDA 510(k) (5 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Litton Datamedix's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Litton Datamedix's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Litton Datamedix in the registry?
The most recently registered devices listed for Litton Datamedix include LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI, ULTRASOUND GEL, SERVOCARD SCP-840 and SERVOMED OXYMONITO SMK 363.