Gynetech, Inc.
Country not established
- Devices
- 1
What Gynetech, Inc. makes
Gynetech, Inc. manufactures the GYNETECH P.O.S. SPAP Smear Cell Collection & Transport Kit, a device designed for collecting and transporting cervical cell samples for diagnostic testing in point-of-service settings.
The company’s product portfolio is regulated under Class II devices in the United States and is listed in the FDA’s 510(k) clearance registry. The manufacturer operates from the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gynetech, Inc. have in the registry?
The registry currently lists 1 device for Gynetech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gynetech, Inc.'s devices?
Among its 1 most recently registered device, Gynetech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Gynetech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gynetech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gynetech, Inc. in the registry?
The most recently registered devices listed for Gynetech, Inc. include GYNETECH P.O.S. SPAP SMEAR CELL COLLECTION & TRANSPORT KIT.