Barnard and Assoc.
Country not established
- Devices
- 1
What Barnard and Assoc. makes
Barnard and Assoc. remanufactures general-purpose, vacuum, or laboratory sterilizers designed for medical, dental, or research environments to meet sterilization standards.
The company’s remanufactured sterilizers are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. The manufacturer operates in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Barnard and Assoc. have in the registry?
The registry currently lists 1 device for Barnard and Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Barnard and Assoc.'s devices?
Among its 1 most recently registered device, Barnard and Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Barnard and Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Barnard and Assoc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Barnard and Assoc. in the registry?
The most recently registered devices listed for Barnard and Assoc. include BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER.