Biocontrol Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Biocontrol Technology, Inc. makes
Biocontrol Technology, Inc. manufactures vascular access systems, specifically the Theraport low-profile and standard models. The company also produces the Neurocontrol Freehand system.
The company is based in the US, and its product portfolio includes devices regulated as Class II and Class III. These devices are listed in the FDA 510(k) and FDA PMA regulatory databases.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Neurocontrol Freehand System Ref P950035
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Biocontrol Technology, Inc. have in the registry?
The registry currently lists 3 devices for Biocontrol Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biocontrol Technology, Inc.'s devices?
Among its 3 most recently registered devices, Biocontrol Technology, Inc. has devices listed in FDA 510(k) (2 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Biocontrol Technology, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Biocontrol Technology, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Biocontrol Technology, Inc. in the registry?
The most recently registered devices listed for Biocontrol Technology, Inc. include THERAPORT LOW-PROFILE VASCULAR ACCESS SYSTEM MODELS 1011 AND 1012, THERAPORT VASCULAR ACCESS SYSTEM; MODEL 1001, 1002, 1601, 1602 and NEUROCONTROL FREEHAND SYSTEM.