Srmc Co., Ltd.
Country not established
- Devices
- 1
What Srmc Co., Ltd. makes
Srmc Co., Ltd. manufactures the MIDI-SRS, a medical device designed for specific diagnostic or therapeutic applications within its class.
The MIDI-SRS is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Midi-Srs Ref K141046
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Srmc Co., Ltd. have in the registry?
The registry currently lists 1 device for Srmc Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Srmc Co., Ltd.'s devices?
Among its 1 most recently registered device, Srmc Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Srmc Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Srmc Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Srmc Co., Ltd. in the registry?
The most recently registered devices listed for Srmc Co., Ltd. include MIDI-SRS.