P.K. Morgan Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What P.K. Morgan Instruments, Inc. makes
P.K. Morgan Instruments, Inc. manufactures portable spirometers for measuring lung function and time-based rhythm clocks designed to assist with medication adherence. These devices are intended for use in clinical and home settings to monitor respiratory health and support treatment schedules.
The company’s products are regulated under FDA’s Class II and Class U device classifications, with spirometers authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) clearance registry, and the manufacturer operates from the United States.
Catalogue
Pocket Spirometer Ref K830995
510(k) 510(k)Right Time Rhythm Clock Ref K823463
510(k) 510(k)
Frequently asked questions
How many devices does P.K. Morgan Instruments, Inc. have in the registry?
The registry currently lists 2 devices for P.K. Morgan Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list P.K. Morgan Instruments, Inc.'s devices?
Among its 2 most recently registered devices, P.K. Morgan Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do P.K. Morgan Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for P.K. Morgan Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from P.K. Morgan Instruments, Inc. in the registry?
The most recently registered devices listed for P.K. Morgan Instruments, Inc. include POCKET SPIROMETER and RIGHT TIME RHYTHM CLOCK.