Symcon Intl., Inc.
Country not established
- Devices
- 1
What Symcon Intl., Inc. makes
Symcon Intl., Inc. manufactures the DIA STRIPS SYSTEM, MODIFIED, a diagnostic device used for detecting specific substances in urine samples, commonly employed in medical settings for rapid testing.
The company’s portfolio is regulated under Class II devices in the US and is listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Dia Strips System, Modified Ref K921495
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Symcon Intl., Inc. have in the registry?
The registry currently lists 1 device for Symcon Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Symcon Intl., Inc.'s devices?
Among its 1 most recently registered device, Symcon Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Symcon Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Symcon Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Symcon Intl., Inc. in the registry?
The most recently registered devices listed for Symcon Intl., Inc. include DIA STRIPS SYSTEM, MODIFIED.