Alan Penn & Associates., Inc.
Country not established
- Devices
- 1
What Alan Penn & Associates., Inc. makes
Alan Penn & Associates, Inc. develops the CADIMAS Version 1.0, a software tool designed for cardiac device analysis and management, including diagnostic and monitoring functions for implantable cardiac devices.
The CADIMAS Version 1.0 is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Cadimas Version 1.0 Ref K052023
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alan Penn & Associates., Inc. have in the registry?
The registry currently lists 1 device for Alan Penn & Associates., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alan Penn & Associates., Inc.'s devices?
Among its 1 most recently registered device, Alan Penn & Associates., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Alan Penn & Associates., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Alan Penn & Associates., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alan Penn & Associates., Inc. in the registry?
The most recently registered devices listed for Alan Penn & Associates., Inc. include CADIMAS VERSION 1.0.