Scripps Laboratories, Inc.
Country not established
- Devices
- 1
What Scripps Laboratories, Inc. makes
Scripps Laboratories, Inc. manufactures the Scripps Laboratories HCG One-Step, a rapid diagnostic test designed for the qualitative detection of human chorionic gonadotropin (hCG) in urine to confirm pregnancy.
This product is classified as a Class II medical device in the United States and is listed under the FDA’s 510(k) clearance process. The company is based in the US.
Catalogue
Scripps Laboratories Hcg One-Step Ref K962906
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scripps Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Scripps Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scripps Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Scripps Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Scripps Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Scripps Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scripps Laboratories, Inc. in the registry?
The most recently registered devices listed for Scripps Laboratories, Inc. include SCRIPPS LABORATORIES HCG ONE-STEP.