L&M Ultrascope Life Monitoring Sys.
Country not established
- Devices
- 2
What L&M Ultrascope Life Monitoring Sys. makes
L&M Ultrascope Life Monitoring Systems manufactures the ULTRASCOPE, a medical device for monitoring vital signs, alongside a SPEAKER-AMPLIFIER & RECORDER INTERFACE for audio recording and playback in clinical settings. These products are designed to support real-time patient observation and documentation in healthcare environments.
The company’s devices fall under Class II regulatory classification in the US, with records submitted via FDA 510(k) clearance. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with US medical device regulations. The manufacturer is based in the United States.
Catalogue
Ultrascope Ref K780200
Regimes: 510(k) Registry: 510(k)Speaker-Amplifier & Recorder Interface Ref K780201
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does L&M Ultrascope Life Monitoring Sys. have in the registry?
The registry currently lists 2 devices for L&M Ultrascope Life Monitoring Sys.. Devices recorded under merged duplicate company entries are counted once.
Which registries list L&M Ultrascope Life Monitoring Sys.'s devices?
Among its 2 most recently registered devices, L&M Ultrascope Life Monitoring Sys. has devices listed in FDA 510(k) (2 devices).
What risk classes do L&M Ultrascope Life Monitoring Sys.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for L&M Ultrascope Life Monitoring Sys.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from L&M Ultrascope Life Monitoring Sys. in the registry?
The most recently registered devices listed for L&M Ultrascope Life Monitoring Sys. include ULTRASCOPE and SPEAKER-AMPLIFIER & RECORDER INTERFACE.