Morgan Associates, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Morgan Associates, Inc. makes
Morgan Associates, Inc. manufactures the Morgan Transcutaneous Electrical Nerve Stimulator, a device for delivering electrical stimulation through the skin to nerves, and the JP-2 Respiratory Monitoring System, which provides continuous monitoring of respiratory parameters.
Both devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Jp-2 Respiratory Monitoring System Ref K832005
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Morgan Associates, Inc. have in the registry?
The registry currently lists 2 devices for Morgan Associates, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Morgan Associates, Inc.'s devices?
Among its 2 most recently registered devices, Morgan Associates, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Morgan Associates, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Morgan Associates, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Morgan Associates, Inc. in the registry?
The most recently registered devices listed for Morgan Associates, Inc. include MORGAN TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR and JP-2 RESPIRATORY MONITORING SYSTEM.