Melville Software, Ltd.
CanadaFDA applicant, unverified
- Devices
- 2
What Melville Software, Ltd. makes
Melville Software, Ltd. manufactures the MMC Amplifier, a device designed for medical imaging signal amplification, and the Sandman, a system used for patient monitoring and sedation management in procedural settings.
The company’s portfolio is regulated under Class II medical devices in the US, with products authorised via the FDA’s 510(k) clearance pathway. Melville Software, Ltd. is based in the United States.
Catalogue
Mmc Amplifier Ref K943673
Regimes: 510(k) Registry: 510(k)Sandman Ref K934599
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Melville Software, Ltd. have in the registry?
The registry currently lists 2 devices for Melville Software, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Melville Software, Ltd.'s devices?
Among its 2 most recently registered devices, Melville Software, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Melville Software, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Melville Software, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Melville Software, Ltd. in the registry?
The most recently registered devices listed for Melville Software, Ltd. include MMC AMPLIFIER and SANDMAN.