Parasitic Disease Consultants
Country not established
- Devices
- 3
What Parasitic Disease Consultants makes
Parasitic Disease Consultants manufactures serological diagnostic tests for syphilis detection, including the Polychaco FIA-ABS Test for Syphilis, as well as indirect hemagglutination and immunofluorescence assays for antibody detection.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Polychaco Fia-Abs Test For Syphilis Ref K831296
Regimes: 510(k) Registry: 510(k)Polychaco Indirect Hemagglutination Ref K830870
Regimes: 510(k) Registry: 510(k)Polychaco Indirect Immunofluorescence Ref K830869
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Parasitic Disease Consultants have in the registry?
The registry currently lists 3 devices for Parasitic Disease Consultants. Devices recorded under merged duplicate company entries are counted once.
Which registries list Parasitic Disease Consultants's devices?
Among its 3 most recently registered devices, Parasitic Disease Consultants has devices listed in FDA 510(k) (3 devices).
What risk classes do Parasitic Disease Consultants's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Parasitic Disease Consultants's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Parasitic Disease Consultants in the registry?
The most recently registered devices listed for Parasitic Disease Consultants include POLYCHACO FIA-ABS TEST FOR SYPHILIS, POLYCHACO INDIRECT HEMAGGLUTINATION and POLYCHACO INDIRECT IMMUNOFLUORESCENCE.