Pathfinder Intl. Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Pathfinder Intl. Corp. makes
Pathfinder Intl. Corp. manufactures a portable medical device labeled PM, designed for specific clinical applications, as well as closed urinary drainage units for managing urinary output in patients.
The company’s portfolio includes devices classified under Class I and Class II per FDA regulations, with products listed via the 510(k) premarket notification process. The manufacturer is based in the United States.
Catalogue
Pm Ref K925980
Regimes: 510(k) Registry: 510(k)Closed Urinary Drainage Unit Ref K843698
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pathfinder Intl. Corp. have in the registry?
The registry currently lists 2 devices for Pathfinder Intl. Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pathfinder Intl. Corp.'s devices?
Among its 2 most recently registered devices, Pathfinder Intl. Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pathfinder Intl. Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pathfinder Intl. Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pathfinder Intl. Corp. in the registry?
The most recently registered devices listed for Pathfinder Intl. Corp. include PM and CLOSED URINARY DRAINAGE UNIT.