Digit-Pro
Country not established
- Devices
- 1
What Digit-Pro makes
Digit-Pro manufactures the PERCUGUARD, a medical device designed for percutaneous procedures to prevent contrast agent extravasation during imaging studies.
The PERCUGUARD is classified as Class I under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
Percuguard Ref K992539
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Digit-Pro have in the registry?
The registry currently lists 1 device for Digit-Pro. Devices recorded under merged duplicate company entries are counted once.
Which registries list Digit-Pro's devices?
Among its 1 most recently registered device, Digit-Pro has devices listed in FDA 510(k) (1 device).
What risk classes do Digit-Pro's devices fall under?
Among its 1 most recently registered device, the classes recorded for Digit-Pro's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Digit-Pro in the registry?
The most recently registered devices listed for Digit-Pro include PERCUGUARD.