Marvic Interpharma, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Marvic Interpharma, Inc. makes
Marvic Interpharma, Inc. manufactures the VES-TEC and VES-MATIC devices, which are designed for vascular access applications, and diagnostic test kits—including the DIESSE CRP and DIESSE RF test kits—for detecting C-reactive protein and rheumatoid factor levels in patient samples.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Ves-Tec/Ves-Matic Ref K854223
Regimes: 510(k) Registry: 510(k)Diesse Crp Test Kit Ref K854221
Regimes: 510(k) Registry: 510(k)Diesse Rf Test Kit Ref K854222
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Marvic Interpharma, Inc. have in the registry?
The registry currently lists 3 devices for Marvic Interpharma, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Marvic Interpharma, Inc.'s devices?
Among its 3 most recently registered devices, Marvic Interpharma, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Marvic Interpharma, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Marvic Interpharma, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Marvic Interpharma, Inc. in the registry?
The most recently registered devices listed for Marvic Interpharma, Inc. include VES-TEC/VES-MATIC, DIESSE CRP TEST KIT and DIESSE RF TEST KIT.