Syncor International, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Syncor International, Inc. makes
Syncor International, Inc. manufactures PharmaSeed devices, including the BT-125-2 and BT-103-2 models, which are designed for pharmaceutical seed coating applications in controlled environments.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Pharmaseed, Model Bt-125-2 Ref K993701
510(k) 510(k)Pharmaseed, Model Bt-103-2 Ref K993700
510(k) 510(k)
Frequently asked questions
How many devices does Syncor International, Inc. have in the registry?
The registry currently lists 2 devices for Syncor International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Syncor International, Inc.'s devices?
Among its 2 most recently registered devices, Syncor International, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Syncor International, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Syncor International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Syncor International, Inc. in the registry?
The most recently registered devices listed for Syncor International, Inc. include PHARMASEED, MODEL BT-125-2 and PHARMASEED, MODEL BT-103-2.