Modern Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Modern Diagnostics, Inc. makes
Modern Diagnostics, Inc. manufactures in vitro diagnostic tests for pregnancy detection, including microtitration assays and early pregnancy screening systems, as well as enzyme-linked immunoassays for antinuclear antibody screening.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Beta-Hcg Microtiter Pregnancy Test Ref K853258
Regimes: 510(k) Registry: 510(k)Pregna/Test Ref K853269
Regimes: 510(k) Registry: 510(k)Enzyme Antinuclear Antibody Screening Test Ref K852840
Regimes: 510(k) Registry: 510(k)Antinuclear Antibody Test Kit Ref K851369
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Modern Diagnostics, Inc. have in the registry?
The registry currently lists 5 devices for Modern Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Modern Diagnostics, Inc.'s devices?
Among its 5 most recently registered devices, Modern Diagnostics, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Modern Diagnostics, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Modern Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Modern Diagnostics, Inc. in the registry?
The most recently registered devices listed for Modern Diagnostics, Inc. include BETA-HCG MICROTITER PREGNANCY TEST, PREGNA/TEST, ENZYME ANTINUCLEAR ANTIBODY SCREENING TEST and ANTINUCLEAR ANTIBODY TEST KIT.