Integrity Practice Management, Inc.
Country not established
- Devices
- 1
What Integrity Practice Management, Inc. makes
Integrity Practice Management, Inc. manufactures the AMI1200 C-arm, a mobile fluoroscopic imaging system designed for intraoperative and procedural radiography in surgical and diagnostic settings.
The AMI1200 C-arm is classified as a Class II medical device under FDA regulations and is supported by a 510(k) clearance. The company is based in the United States.
Catalogue
Model AMI1200 C-Arm Ref K022911
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Integrity Practice Management, Inc. have in the registry?
The registry currently lists 1 device for Integrity Practice Management, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Integrity Practice Management, Inc.'s devices?
Among its 1 most recently registered device, Integrity Practice Management, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Integrity Practice Management, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Integrity Practice Management, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Integrity Practice Management, Inc. in the registry?
The most recently registered devices listed for Integrity Practice Management, Inc. include MODEL AMI1200 C-ARM.