Squibb Diagnostics
Country not established
- Devices
- 3
What Squibb Diagnostics makes
Squibb Diagnostics manufactures medical devices including a radionuclide infusion system for diagnostic imaging, an electrosurgical system called the Biceps Electrocautery System for tissue cutting and coagulation, and an accessory package designed for use with the CardioGen-82 generator.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Radionuclide Infusion System Ref K842568
Regimes: 510(k) Registry: 510(k)Biceps Electrocautery System Ref K823755
Regimes: 510(k) Registry: 510(k)Acces. Package For Use W/Cardiogen-82 Generator Ref K883609
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Squibb Diagnostics have in the registry?
The registry currently lists 3 devices for Squibb Diagnostics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Squibb Diagnostics's devices?
Among its 3 most recently registered devices, Squibb Diagnostics has devices listed in FDA 510(k) (3 devices).
What risk classes do Squibb Diagnostics's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Squibb Diagnostics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Squibb Diagnostics in the registry?
The most recently registered devices listed for Squibb Diagnostics include RADIONUCLIDE INFUSION SYSTEM, BICEPS ELECTROCAUTERY SYSTEM and ACCES. PACKAGE FOR USE W/CARDIOGEN-82 GENERATOR.