Vicor Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Vicor Technologies, Inc. makes
Vicor Technologies, Inc. manufactures the VICOR PD2I Analyzer and its updated version, VICOR PD2I Analyzer Version 2.1, which are diagnostic devices designed for evaluating platelet dysfunction and coagulation parameters in blood samples.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Vicor PD2I Analyzer Ref K101867
Regimes: 510(k) Registry: 510(k)Vicor PD2I Analyzer, Version 2.1 Ref K082709
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vicor Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Vicor Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vicor Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Vicor Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Vicor Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vicor Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vicor Technologies, Inc. in the registry?
The most recently registered devices listed for Vicor Technologies, Inc. include VICOR PD2I ANALYZER and VICOR PD2I ANALYZER, VERSION 2.1.