Rigel Medical Electronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Rigel Model Multicare 409 Ref K875160
Regimes: 510(k) Registry: 510(k)Ecg Patient Monitor 302 Ref K850155
Regimes: 510(k) Registry: 510(k)Ecg Patient Monitor 301 Ref K850156
Regimes: 510(k) Registry: 510(k)Neonatal Monitor 309 Ref K850407
Regimes: 510(k) Registry: 510(k)Ecg Patient Monitor Ref K843376
Regimes: 510(k) Registry: 510(k)Patient Monitor Rigel Model Multicare 429 Ref K884645
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rigel Medical Electronics, Inc. have in the registry?
The registry currently lists 6 devices for Rigel Medical Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rigel Medical Electronics, Inc.'s devices?
Among its 6 most recently registered devices, Rigel Medical Electronics, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Rigel Medical Electronics, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Rigel Medical Electronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rigel Medical Electronics, Inc. in the registry?
The most recently registered devices listed for Rigel Medical Electronics, Inc. include RIGEL MODEL MULTICARE 409, ECG PATIENT MONITOR 302, ECG PATIENT MONITOR 301 and NEONATAL MONITOR 309.