Callisyn Biomedical, Inc.
Country not established
- Devices
- 1
What Callisyn Biomedical, Inc. makes
Callisyn Biomedical, Inc. makes the FluidiTube 2.7F Infusion Micro Catheter, available in 110 cm and 130 cm lengths.
This device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Callisyn Biomedical, Inc. have in the registry?
The registry currently lists 1 device for Callisyn Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Callisyn Biomedical, Inc.'s devices?
Among its 1 most recently registered device, Callisyn Biomedical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Callisyn Biomedical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Callisyn Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Callisyn Biomedical, Inc. in the registry?
The most recently registered devices listed for Callisyn Biomedical, Inc. include FluidiTube 2.7F Infusion Micro Catheter, 110 cm and 130 cm.