California Medical Developments, Inc.
Country not established
- Devices
- 1
What California Medical Developments, Inc. makes
California Medical Developments, Inc. manufactures the Drugalyzer DTK-1000 Kit, a presumptive drug detection device designed for rapid on-site testing of bodily fluids to identify the presence of controlled substances.
The company’s portfolio is regulated under FDA’s Class II device classification, with the Drugalyzer DTK-1000 Kit authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Drugalyzer Dtk-1000 Kit Presumptive Drug Ref K792282
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does California Medical Developments, Inc. have in the registry?
The registry currently lists 1 device for California Medical Developments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list California Medical Developments, Inc.'s devices?
Among its 1 most recently registered device, California Medical Developments, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do California Medical Developments, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for California Medical Developments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from California Medical Developments, Inc. in the registry?
The most recently registered devices listed for California Medical Developments, Inc. include DRUGALYZER DTK-1000 KIT PRESUMPTIVE DRUG.