Perstorp Ab C/O Robert Joel Slomoff
Country not established
- Devices
- 2
What Perstorp Ab C/O Robert Joel Slomoff makes
Perstorp AB manufactures IODOSORB in powder and gel formulations, designed for use in medical procedures requiring contrast agent absorption or removal.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Iodosorb Powder Ref K870559
Regimes: 510(k) Registry: 510(k)Iodosorb Gel Ref K905069
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perstorp AB C/O Robert Joel Slomoff have in the registry?
The registry currently lists 2 devices for Perstorp AB C/O Robert Joel Slomoff. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perstorp AB C/O Robert Joel Slomoff's devices?
Among its 2 most recently registered devices, Perstorp AB C/O Robert Joel Slomoff has devices listed in FDA 510(k) (2 devices).
What risk classes do Perstorp AB C/O Robert Joel Slomoff's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Perstorp AB C/O Robert Joel Slomoff's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Perstorp AB C/O Robert Joel Slomoff in the registry?
The most recently registered devices listed for Perstorp AB C/O Robert Joel Slomoff include IODOSORB POWDER and IODOSORB GEL.