Diagnostic Testing, Inc.
Country not established
- Devices
- 1
What Diagnostic Testing, Inc. makes
Diagnostic Testing, Inc. manufactures a pregnancy test kit designed to provide qualitative results for detecting human chorionic gonadotropin (hCG) in urine samples.
The company’s products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer operates from the United States.
Catalogue
Pregnancy Test Kit, Answer Ref K772359
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diagnostic Testing, Inc. have in the registry?
The registry currently lists 1 device for Diagnostic Testing, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diagnostic Testing, Inc.'s devices?
Among its 1 most recently registered device, Diagnostic Testing, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Diagnostic Testing, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Diagnostic Testing, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diagnostic Testing, Inc. in the registry?
The most recently registered devices listed for Diagnostic Testing, Inc. include PREGNANCY TEST KIT, ANSWER.