Qstag, Inc.
South KoreaFDA applicant, unverified
- Devices
- 1
What Qstag, Inc. makes
Qstag, Inc. manufactures the QSCHECK UISACR, a device designed for the verification and testing of urinary catheters, ensuring proper functionality and safety in clinical settings.
The company’s portfolio is regulated under Class II medical devices in the United States, with the QSCHECK UISACR listed via the FDA’s 510(k) clearance process. The manufacturer is based in the US.
Catalogue
Qscheck Uisacr Ref K252619
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Qstag, Inc. have in the registry?
The registry currently lists 1 device for Qstag, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Qstag, Inc.'s devices?
Among its 1 most recently registered device, Qstag, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Qstag, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Qstag, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Qstag, Inc. in the registry?
The most recently registered devices listed for Qstag, Inc. include QSCHECK UISACR.