Laszlo Corp.
Country not established
- Devices
- 1
What Laszlo Corp. makes
Laszlo Corp. manufactures the ZIGGY MEDICHAIR, a Class I medical device designed for patient positioning and support in clinical settings.
The ZIGGY MEDICHAIR is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA registry. The company is based in the United States.
Catalogue
Ziggy Medichair Ref K895165
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laszlo Corp. have in the registry?
The registry currently lists 1 device for Laszlo Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laszlo Corp.'s devices?
Among its 1 most recently registered device, Laszlo Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Laszlo Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Laszlo Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Laszlo Corp. in the registry?
The most recently registered devices listed for Laszlo Corp. include ZIGGY MEDICHAIR.