Canberra Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Canberra Industries, Inc. makes
Canberra Industries, Inc. manufactures medical imaging systems, including the ImageView 46000 series for diagnostic imaging, as well as laboratory devices like the Matrix™-96 for sample analysis. The company also produces fibrinogen uptake systems in multiple models, designed for blood coagulation testing and monitoring.
These devices are regulated under the FDA’s 510(k) pathway, with classifications spanning Class I and Class II. They are listed in the FDA’s 510(k) database, and the company operates from the United States.
Catalogue
Fibrinogen Uptake Sys -Various Models Ref K834168
Regimes: 510(k) Registry: 510(k)Imageview 46000 Ref K925265
Regimes: 510(k) Registry: 510(k)Matrix(Tm)-96 Ref K896202
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Canberra Industries, Inc. have in the registry?
The registry currently lists 3 devices for Canberra Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Canberra Industries, Inc.'s devices?
Among its 3 most recently registered devices, Canberra Industries, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Canberra Industries, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Canberra Industries, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Canberra Industries, Inc. in the registry?
The most recently registered devices listed for Canberra Industries, Inc. include FIBRINOGEN UPTAKE SYS -VARIOUS MODELS, IMAGEVIEW 46000 and MATRIX(TM)-96.