Immunicon Corp.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Celltracks Analyzer Ii Ref K060110
Regimes: 510(k) Registry: 510(k)Celltracka Analyzer Ii Ref K050145
Regimes: 510(k) Registry: 510(k)Cellprep Sample Preparation System, Model 9518 Ref K022512
Regimes: 510(k) Registry: 510(k)Immunicon Cellsave Preservative Tube Ref K030596
Regimes: 510(k) Registry: 510(k)Immunicon Celltracks Autoprep System Ref K040077
Regimes: 510(k) Registry: 510(k)Immunicon Celltracks Analyzer Ref K030263
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Immunicon Corp. have in the registry?
The registry currently lists 6 devices for Immunicon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Immunicon Corp.'s devices?
Among its 6 most recently registered devices, Immunicon Corp. has devices listed in FDA 510(k) (6 devices).
What risk classes do Immunicon Corp.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Immunicon Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Immunicon Corp. in the registry?
The most recently registered devices listed for Immunicon Corp. include CELLTRACKS ANALYZER II, CELLTRACKA ANALYZER II, CELLPREP SAMPLE PREPARATION SYSTEM, MODEL 9518 and IMMUNICON CELLSAVE PRESERVATIVE TUBE.