Skidmore Medical, Limited
Country not established FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Skidmore Medical, Limited makes
Skidmore Medical produces the STUDIODOP VICORDER, a device designed for Doppler ultrasound imaging used in vascular studies to assess blood flow and detect abnormalities in blood vessels.
The company’s portfolio is regulated under Class II devices in the US, with the STUDIODOP VICORDER listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Studiodop Vicorder Ref K071730
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Skidmore Medical Limited Bristol Bristol, City of · GB FEI 3006648308
Frequently asked questions
How many devices does Skidmore Medical, Limited have in the registry?
The registry currently lists 1 device for Skidmore Medical, Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Skidmore Medical, Limited's devices?
Among its 1 most recently registered device, Skidmore Medical, Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Skidmore Medical, Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Skidmore Medical, Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Skidmore Medical, Limited in the registry?
The most recently registered devices listed for Skidmore Medical, Limited include STUDIODOP VICORDER.
Which FDA establishments are linked to Skidmore Medical, Limited?
1 FDA establishment is linked to Skidmore Medical, Limited in the registry; they are listed on the company page.