Pneumrx, Inc.
Country not established
- Devices
- 1
What Pneumrx, Inc. makes
Pneumrx, Inc. manufactures biopsy needles and associated kits designed for medical procedures requiring tissue sampling. These devices are intended for use in diagnostic evaluations where precise tissue acquisition is required, such as in oncology or pathology assessments.
The company’s portfolio is regulated under FDA Class II devices, with individual products authorised through the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Pneumrx Family Of Biopsy Needles And Kits Ref K052435
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pneumrx, Inc. have in the registry?
The registry currently lists 1 device for Pneumrx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pneumrx, Inc.'s devices?
Among its 1 most recently registered device, Pneumrx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pneumrx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pneumrx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pneumrx, Inc. in the registry?
The most recently registered devices listed for Pneumrx, Inc. include PNEUMRX FAMILY OF BIOPSY NEEDLES AND KITS.