Jcl Clinical Research Corp.
Country not established
- Devices
- 1
What Jcl Clinical Research Corp. makes
Jcl Clinical Research Corp. manufactures the Erythropoietin Enzyme Immunoassay (EIA), a diagnostic test used to measure erythropoietin levels in blood samples, typically for clinical research or diagnostic purposes.
The company’s portfolio is regulated under FDA’s Class II device classification, with the EIA listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Erythropoietin Eia Ref K833957
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jcl Clinical Research Corp. have in the registry?
The registry currently lists 1 device for Jcl Clinical Research Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jcl Clinical Research Corp.'s devices?
Among its 1 most recently registered device, Jcl Clinical Research Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Jcl Clinical Research Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jcl Clinical Research Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jcl Clinical Research Corp. in the registry?
The most recently registered devices listed for Jcl Clinical Research Corp. include ERYTHROPOIETIN EIA.