Barton-Carey Medical Products Co.
United Statesfrom the FDA registration address FDA FEI 3003070670
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Barton-Carey Medical Products Co. makes
Barton-Carey Medical Products Co. manufactures the VASC-EZ, a vascular access device designed to facilitate intravenous or intra-arterial catheter insertion.
The company’s portfolio is regulated under FDA Class II devices and includes products listed via the 510(k) premarket notification process. The manufacturer is based in the United States.
Catalogue
Vasc-Ez Ref K854428
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003070670
- Address
- 460 FIFTH ST., JELLICO, TN, 37762
Frequently asked questions
How many devices does Barton-Carey Medical Products Co. have in the registry?
The registry currently lists 1 device for Barton-Carey Medical Products Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Barton-Carey Medical Products Co.'s devices?
Among its 1 most recently registered device, Barton-Carey Medical Products Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Barton-Carey Medical Products Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Barton-Carey Medical Products Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Barton-Carey Medical Products Co. in the registry?
The most recently registered devices listed for Barton-Carey Medical Products Co. include VASC-EZ.