Barbaras Development, Inc.
Country not established FDA establishment FEI 3007207474
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Barbaras Development, Inc. makes
Barbaras Development, Inc. makes CO2 sampling lines, including models 0184, 0184T, 0139, and 0182.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
0184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling line Ref K251216
510(k) 510(k)
Company details
- FDA FEI number
- 3007207474
- Address
- 2545 W Hillcrest Dr Ste 215, Thousand Oaks, CA, 91320
Frequently asked questions
How many devices does BARBARAS DEVELOPMENT, INC. have in the registry?
The registry currently lists 1 device for BARBARAS DEVELOPMENT, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BARBARAS DEVELOPMENT, INC.'s devices?
Among its 1 most recently registered device, BARBARAS DEVELOPMENT, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do BARBARAS DEVELOPMENT, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for BARBARAS DEVELOPMENT, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from BARBARAS DEVELOPMENT, INC. in the registry?
The most recently registered devices listed for BARBARAS DEVELOPMENT, INC. include 0184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling line.