Microgon, Inc.
Country not established
- Devices
- 1
What Microgon, Inc. makes
Microgon, Inc. manufactures the Dyna Gard syringe filter, a device designed to remove particulate matter and bacteria from liquid medications during preparation or administration.
The Dyna Gard syringe filter is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Dyna Gard Syringe Filter Ref K852996
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microgon, Inc. have in the registry?
The registry currently lists 1 device for Microgon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microgon, Inc.'s devices?
Among its 1 most recently registered device, Microgon, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Microgon, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Microgon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microgon, Inc. in the registry?
The most recently registered devices listed for Microgon, Inc. include DYNA GARD SYRINGE FILTER.