P.K. Morgan, Ltd.
United KingdomFDA 510(k) applicant, unverified
- Devices
- 4
What P.K. Morgan, Ltd. makes
P.K. Morgan, Ltd. manufactures respiratory diagnostic equipment, including the OXYLOG 2, the AUTOLINK body plethysmograph, the BENCHMARK transfer test, and the TRANSFLOW test.
The company is based in the US, and its portfolio consists of Class II medical devices that are listed in the FDA 510(k) registry.
Catalogue
Oxylog 2 Ref K954731
510(k) 510(k)Autolink Body Plethysmograph Ref K960121
510(k) 510(k)Benchmark Transfer Test Ref K954730
510(k) 510(k)Transflow Test Ref K953990
510(k) 510(k)
Frequently asked questions
How many devices does P.K. Morgan, Ltd. have in the registry?
The registry currently lists 4 devices for P.K. Morgan, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list P.K. Morgan, Ltd.'s devices?
Among its 4 most recently registered devices, P.K. Morgan, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do P.K. Morgan, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for P.K. Morgan, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from P.K. Morgan, Ltd. in the registry?
The most recently registered devices listed for P.K. Morgan, Ltd. include OXYLOG 2, AUTOLINK BODY PLETHYSMOGRAPH, BENCHMARK TRANSFER TEST and TRANSFLOW TEST.