Zelby, Burstein, Hartman & Burstein
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- Devices
- 1
What Zelby, Burstein, Hartman & Burstein makes
Zelby, Burstein, Hartman & Burstein makes the PISTORMATIC device.
The PISTORMATIC is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Pistormatic Ref K790104
510(k) 510(k)
Frequently asked questions
How many devices does Zelby, Burstein, Hartman & Burstein have in the registry?
The registry currently lists 1 device for Zelby, Burstein, Hartman & Burstein. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zelby, Burstein, Hartman & Burstein's devices?
Among its 1 most recently registered device, Zelby, Burstein, Hartman & Burstein has devices listed in FDA 510(k) (1 device).
What risk classes do Zelby, Burstein, Hartman & Burstein's devices fall under?
Among its 1 most recently registered device, the classes recorded for Zelby, Burstein, Hartman & Burstein's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zelby, Burstein, Hartman & Burstein in the registry?
The most recently registered devices listed for Zelby, Burstein, Hartman & Burstein include PISTORMATIC.