RQMIS, Inc.
Country not established
- Devices
- 1
What RQMIS, Inc. makes
RQMIS, Inc. manufactures the AccuMeasure System, a medical device designed for precise measurement and monitoring in clinical settings, likely supporting diagnostic or procedural workflows.
The AccuMeasure System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
AccuMeasure System Ref DEN210032
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does RQMIS, Inc. have in the registry?
The registry currently lists 1 device for RQMIS, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list RQMIS, Inc.'s devices?
Among its 1 most recently registered device, RQMIS, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do RQMIS, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for RQMIS, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from RQMIS, Inc. in the registry?
The most recently registered devices listed for RQMIS, Inc. include AccuMeasure System.