Sunscope Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Heparin Coated Thermodilution Cath & Accessories Ref K911710
Regimes: 510(k) Registry: 510(k)Biosensors Central Venous Catheter Kits Ref K002786
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Biosensors Embolectomy Catheter Ref K973477
Regimes: 510(k) Registry: 510(k)Safewedge(Tm) Relief Valve Device Ref K912172
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sunscope Intl., Inc. have in the registry?
The registry currently lists 7 devices for Sunscope Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sunscope Intl., Inc.'s devices?
Among its 7 most recently registered devices, Sunscope Intl., Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Sunscope Intl., Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Sunscope Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sunscope Intl., Inc. in the registry?
The most recently registered devices listed for Sunscope Intl., Inc. include BIOPORT CLOSED BLOOD SAMPLING SYSTEM, MODEL BT XXXXXX- BP, HEPARIN COATED THERMODILUTION CATH & ACCESSORIES, BIOSENSORS CENTRAL VENOUS CATHETER KITS and BIOTRANS REUSABLE SENSOR BASE MODEL NUMBER BT XXXXXX.