B&J Manufacturing, Ltd.
ChinaFDA 510(k) applicant, unverified
- Devices
- 4
Catalogue
B&J DVT Foot Garments, Models 820 Series Ref K201547
510(k) 510(k)- 510(k) 510(k)
B&J DVT Compression Devices MHH800/MHH800SQ Ref K200154
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does B&J Manufacturing, Ltd. have in the registry?
The registry currently lists 4 devices for B&J Manufacturing, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list B&J Manufacturing, Ltd.'s devices?
Among its 4 most recently registered devices, B&J Manufacturing, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do B&J Manufacturing, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for B&J Manufacturing, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from B&J Manufacturing, Ltd. in the registry?
The most recently registered devices listed for B&J Manufacturing, Ltd. include B&J DVT Foot Garments, Models 820 Series, B&J DVT Calf/Thigh Garments, Models 801/830 Series, B&J DVT Compression Devices MHH800/MHH800SQ and B&J MHP800 Deep Vein Thrombosis (DVT) Prevention System.