Diversified Diagnostic Industries
Country not established
- Devices
- 3
What Diversified Diagnostic Industries makes
Diversified Diagnostic Industries manufactures chromagen-based test kits for bacterial identification, including differentiation of Gram-positive and Gram-negative bacteria, detection of Group D Enterococcus, and identification of Group A Streptococcus. These tests are designed for laboratory use to aid in rapid and accurate microbial identification.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are intended for use within the United States, adhering to applicable regulatory standards for diagnostic testing.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Chromagen Test For Group D Enterococcus Ref K870410
Regimes: 510(k) Registry: 510(k)Chromagen Test For Group A Strep Ref K870409
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diversified Diagnostic Industries have in the registry?
The registry currently lists 3 devices for Diversified Diagnostic Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diversified Diagnostic Industries's devices?
Among its 3 most recently registered devices, Diversified Diagnostic Industries has devices listed in FDA 510(k) (3 devices).
What risk classes do Diversified Diagnostic Industries's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Diversified Diagnostic Industries's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Diversified Diagnostic Industries in the registry?
The most recently registered devices listed for Diversified Diagnostic Industries include CHROMAGEN TEST FOR GRAM (+) & (-) DIFFERENTIATION, CHROMAGEN TEST FOR GROUP D ENTEROCOCCUS and CHROMAGEN TEST FOR GROUP A STREP.