Duoject Medical Systems, Inc.
CanadaFDA 510(k) applicant, unverified
- Devices
- 3
Catalogue
Smart-Rod Ref K070584
510(k) 510(k)E-Z Link Ref K133097
510(k) 510(k)Inter-Vial Ref K010703
510(k) 510(k)
Frequently asked questions
How many devices does Duoject Medical Systems, Inc. have in the registry?
The registry currently lists 3 devices for Duoject Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Duoject Medical Systems, Inc.'s devices?
Among its 3 most recently registered devices, Duoject Medical Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Duoject Medical Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Duoject Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Duoject Medical Systems, Inc. in the registry?
The most recently registered devices listed for Duoject Medical Systems, Inc. include SMART-ROD, E-Z LINK and INTER-VIAL.