The Minnesota Back Brace Co.
Country not established
- Devices
- 1
What The Minnesota Back Brace Co. makes
The Minnesota Back Brace Co. manufactures catheters specifically for mediastinal and pericardial use.
Their products are Class II devices listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
Catheter, Mediastinal&Pericardial Ref K771986
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Minnesota Back Brace Co. have in the registry?
The registry currently lists 1 device for The Minnesota Back Brace Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Minnesota Back Brace Co.'s devices?
Among its 1 most recently registered device, The Minnesota Back Brace Co. has devices listed in FDA 510(k) (1 device).
What risk classes do The Minnesota Back Brace Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Minnesota Back Brace Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Minnesota Back Brace Co. in the registry?
The most recently registered devices listed for The Minnesota Back Brace Co. include CATHETER, MEDIASTINAL&PERICARDIAL.