Dass, Inc.
Country not established
- Devices
- 1
What Dass, Inc. makes
Dass, Inc. manufactures the DASS PACK, a Class I medical device designed for [specific use not detailed in provided data].
The DASS PACK is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Dass Pack Ref K851280
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dass, Inc. have in the registry?
The registry currently lists 1 device for Dass, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dass, Inc.'s devices?
Among its 1 most recently registered device, Dass, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dass, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dass, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dass, Inc. in the registry?
The most recently registered devices listed for Dass, Inc. include DASS PACK.