Clinicomp, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Clinicomp, Inc. makes
Clinicomp, Inc. develops software for managing radionuclide dispensing and clinical information systems, including remote fetal monitoring distribution features. Their portfolio also includes a radiopharmaceutical compounding information system (R.C.I.) for tracking and documentation purposes.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the 510(k) clearance database. Clinicomp, Inc. is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Clinicomp R.C.I. Ref K842540
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinicomp, Inc. have in the registry?
The registry currently lists 3 devices for Clinicomp, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinicomp, Inc.'s devices?
Among its 3 most recently registered devices, Clinicomp, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Clinicomp, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Clinicomp, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinicomp, Inc. in the registry?
The most recently registered devices listed for Clinicomp, Inc. include CLINICOMP RDMS RADIONUCLIDE DISPENSING MGMT. SOFTW, CLINICAL INFOR SYST(CIS) W/FETAL MONIT REMOTE DISP and CLINICOMP R.C.I..