Radiation Development Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Radiation Development Co., Inc. makes
Radiation Development Co., Inc. manufactures bone marrow biopsy devices and Lee aspiration needles, which are designed for obtaining tissue samples and fluid aspiration in clinical settings.
These products are classified as Class I medical devices and are listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Bone Marrow Biopsy Device Ref K772293
Regimes: 510(k) Registry: 510(k)Lee Aspiration Needle Ref K771574
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radiation Development Co., Inc. have in the registry?
The registry currently lists 2 devices for Radiation Development Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Radiation Development Co., Inc.'s devices?
Among its 2 most recently registered devices, Radiation Development Co., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Radiation Development Co., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Radiation Development Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Radiation Development Co., Inc. in the registry?
The most recently registered devices listed for Radiation Development Co., Inc. include BONE MARROW BIOPSY DEVICE and LEE ASPIRATION NEEDLE.